Clinical trials

189

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Withdrawal of Dupilumab in Severe Asthma

Asthma management has been revolutionised by the development of biological therapies. Dupilumab is an anti-interleukin4 receptor marketed in 2020 for severe asthmatic patients with 2 exacerbations or more within the last 12 months. Although data showed that safety and efficacy of dupilumab are sustained when treatment is extended up to 3 years, no study has emerged regarding dupilumab discontinuation. This study aims to demonstrate the non-inferiority regarding strategy failure at 24 months of stopping dupilumab (intervention group) compared with its continuation (control group) in controlled asthma patients receiving this drug for at least 3 years.

Participants needed: 205
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Oct 8, 2026Locations: 29
Eligibility criteria

Adult patients ≥ 18 years old [+2]

Patients who refuse to discontinue dupilumab, for any reason [+6]

Status: Not yet recruiting

Comparative Analysis of Labor Induction Using a Balloon Catheter at Home Versus in the Hospital

An increasing proportion of patients undergo labor induction at the end of pregnancy. Balloon induction at home is a method validated in the literature. Home-based balloon induction is already part of routine care at the Paule de Viguier maternity unit. However, a prospective evaluation of this home induction option has not yet been conducted at our facility or elsewhere in France. Our study will evaluate obstetric outcomes and patient satisfaction regarding this induction method at our center. This is an observational, non-interventional, prospective, and comparative-though non-randomized-study.

Participants needed: 100
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: University Hospital, ToulouseUpdated: Sep 30, 2026Locations: 1Duration: 6 Days
Eligibility criteria

Medical indication or request for induction [+5]

Scarred uterus [+8]

Status: Not yet recruiting

Study on the Prevention of Weight Loss Through Physical Activity Among Nursing Home Residents

Appetite loss is frequent in institutionalized older adults. Physical activity is known for its benefits on appetite regulation but its effects in nursing home residents remain poorly investigated. This project will investigate the 6-month longitudinal relationships between daily physical activity time with appetite and bodyweight and how engaging in a 6-month regular exercise program can improve theses outcomes in older institutionalized older adults.

Participants needed: 596
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Be a resident in a nursing home (EHPAD). [+5]

Unstable cardiovascular disease or any other health condition contraindicating p... [+3]

Status: Not yet recruiting

Effect of Botulinum Toxin on Resting Tremor of the Refractory Upper Limb in Parkinsonians

Tremor is one of the most common symptoms in Parkinson Disease (PD), affecting almost 60% of patients. There is currently no specific treatment for tremor in PD, and 30% of patients develop drug-resistant tremor, making its management more complex. Botulinum toxin (BT) is widely used in neurology, but few studies have been carried out on the effect of BT in parkinsonian tremor without consensus on its management in parkinsonian patients. In this study, the investigators therefore propose to evaluate the effect of BT injected using precision medicine in the treatment of refractory resting tremor in patients with PD, compared with placebo injection.

Participants needed: 39
Trial details
Phase: Phase 3Age: 40-80Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Sep 22, 2026Locations: 2
Eligibility criteria

Patients with PD defined according to UKPDSBB criteria; [+6]

Patients with tremors related to a pathology other than PD; [+10]

Status: Recruiting

Contamination of Young Children Hair During Acute Cannabis Intoxication

Hair analysis in pediatric cannabis intoxication is limited by possible sudoral self-contamination, especially in young children due to hair porosity. However, adult studies show no THC-COOH in sweat, challenging this hypothesis. THC-COOH presence in sweat has to this day never been studied in young children. Its absence would help assess the reliability of hair testing for prior exposure. Thus, our main objective is to describe whether THC-COOH can be detected in sweat following cannabis intoxication using gold standard techniques.

Participants needed: 15
Trial details
Age: 3-3Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Child admitted to the Specialized Emergency Pole (POSU) and pediatric medico-sur... [+2]

History of cannabis intoxication identified during the interview and/or consulta... [+4]

Status: Recruiting

Use of a Social Assistance Robot in a Population of Children Subjected to Prolonged Isolation

During the period of isolation of the hospitalized child, contacts between the child and his family are impaired. Being away from home as well as from the social and family circle can be harmful for the hospitalized child. It seems necessary to measure the impact of the use of such an assistance robot both on the user himself and his family. Thus, it seems relevant to scientifically validate the benefit of using such an assistance robot to break iatrogenic social isolation and to measure the impact of this use.

Participants needed: 33
Trial details
Age: 7-18Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Children hospitalized in the pediatric hemato-oncology department whose duration... [+2]

Patient or two parents who do not have a sufficient level of French for research... [+2]

Status: Recruiting

Optimization of Hearing Performance in the Subject Implanted

In the past two decades, the selection criteria for cochlear implantation have been greatly relaxed so that about 60-70% of present cochlear implant (CI) candidates have significant residual hearing in their contralateral ear. However, contralateral hearing is often not considered in rehabilitation programs, mainly due to the lack of scientific evidence on the role it may play. The present project aims to better understand the mechanisms of perceptual learning of CI-processed speech after implantation and to develop and test rehabilitation strategies for CI users.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Age>18 [+5]

- Subjects under juridical protections or tutelage measure [+2]

Status: Not yet recruiting

TicAgreLor Versus Placebo to Prevent Cerebral ISCHemia in anEuRysmal Low Grade SAH A Double Blinded Randomised Controlled Study

Among aneurysmal subarachnoid hemorrhage (aSAH) survivors, ischemic injuries such as peri procedural thromboembolic events (TEE) and delayed cerebral ischemia (DCI) represent the most important disabling complications. However, preventive strategies are limited. Platelet activation mechanisms play a critical role in the pathophysiology of TEE and DCI. The results of several meta analyses suggested that use of antiplatelet drugs (APD) could reduce the risk of TTE/DCI. We aim to evaluate in patients with a low grade aSAH (WFNS 1 to 3) that occurred for less than 72 hours ago, the effect of 14 days course of ticagrelor vs placebo, initiated at the beginning of the endovascular treatment of the aneurysm, on the ischemic complications (peri-procedural symptomatic and asymptomatic TEE and/or neurological worsening due to DCI) occurring within 14 days of the endovascular treatment of the aneurysm.

Participants needed: 274
Trial details
Phase: Phase 3Age: 18-80Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Sep 15, 2026Locations: 7
Eligibility criteria

Age 18 - 80 years old [+6]

Poor grade aSAH defined as WFNS 4 and 5 [+14]

Status: Not yet recruiting

Comparative Study of Two Vaccination Schedules for the Subunit Herpes Zoster Vaccine in Multiple Sclerosis and Neuromyelitis Optica Spectrum Disease Patients Treated With Anti-CD20 Therapy: an Open-label Randomised Controlled Trial

Immunocompromised individuals, such as patients with multiple sclerosis (MS) or diseases of the neuromyelitis optica spectrum (NMOSD) treated with an anti-CD20 monoclonal antibody, present an increased risk of shingles. The immunogenicity - and therefore the clinical effectiveness - of the recombinant vaccine against the varicella zoster virus based on glycoprotein E, recently recommended according to two-dose schedule two months apart in immunocompromised patients aged ≥ 18 years, could be significantly decreased when administered one month before and one month after the infusion of anti-CD20. We hypothesize that, in patients with MS or NMOSD treated with anti-CD20 administered every six months, a two-dose M0-M6 vaccination schedule consisting of deferring the second dose six months after the first infusion, that is, five months after the anti-CD20 infusion, could improve vaccine immunogenicity and, consequently, the effectiveness of the vaccine.

Participants needed: 160
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Sep 14, 2026Locations: 24
Eligibility criteria

Patients with Multiple Sclerosis (any clinical form) or Neuromyelitis optica spe... [+7]

Temporary contraindication to vaccination (concurrent episode of acute fever >38... [+9]

Status: Not yet recruiting

Study of the Intracerebral Electrophysiological Signature in the Epileptic Patient

As part of the clinical management of certain severe, drug-resistant forms of epilepsy, it is necessary to implant electrodes in the brain to identify the epileptic network prior to potential neurosurgical resection of the source zones. This standardized procedure, known as Stereo-Electroencephalography (SEEG), was developed in France in the 1960s. The electrodes remain implanted for several days-typically two weeks-while awaiting spontaneous epileptic seizures. During this period, the patient remains hospitalized, and their electroencephalographic activity is recorded around the clock. Patients can be asked to perform cognitive tasks (such as tasks involving memory, attention, vision, language, and decision-making) while awake or asleep; the results can then be correlated with the intracerebral electroencephalographic activity recorded simultaneously as part of their clinical care. This approach makes it possible to capture the electrophysiological signatures of specific cognitive processes, thereby enabling researchers to: 1) create a brain map of electrophysiological signatures, 2) improve standard models of cognitive function, and 3) study the dysfunction of these processes in epilepsy.

Participants needed: 75
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Sep 1, 2026Locations: 1Duration: 3 Weeks
Eligibility criteria

Patient with drug-resistant focal epilepsy undergoing SEEG evaluation as part of... [+1]

Patients already participating in another research project that prohibits partic...

Status: Not yet recruiting

mRNA Therapy to Restore Lymphatic Flow in Secondary Lymphedema

Lymphedema is a common complication of breast cancer treatment, affecting approximately a quarter of patients. Those affected can have an uncomfortable, unsightly and sometimes functionally impaired limb prone to episodes of superficial infection. The aetiology and pathophysiology of lymphedema in patients with breast cancer appear to be multifactorial and are still not fully understood.Although conservative treatment techniques can be very successful in controlling symptoms, they do not afford a cure. In this situation of unmet medical need, it is essential to find a new therapeutic solution to treat lymphedema. The approach of the LYMPHARN project is based on dual mRNA strategy delivered by FlashRNA® vector targeting both lymphatic endothelium and surrounding adipose tissue function.

Participants needed: 9
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 28, 2026Locations: 1
Eligibility criteria

Women who developed upper limb lymphedema after surgery for breast cancer hormon... [+7]

HER2+ breast cancer triple positive, [+20]

Status: Recruiting

Restauration of the Auditory and Cognitive Functions in Cochlear Implanted Deaf Children in fNIRS

The principal aim of this study is to evaluate the cortical developement of perceptual skills and executive functions over time, in children with cochlear implants aged 10-24 months and 3-7 years compared with normally hearing subjects (NHS). To do this, the investigator will use functional Near InfraRed Spectroscopy (fNIRS) during 4 tasks that engage the childs perceptual and cognitive skills over a period of 18 months. The performance scores obtained by each participants as well as the cortical activity will be analysed and decrypted.

Participants needed: 80
Trial details
Age: 10-7Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 31, 2026Locations: 1
Eligibility criteria

10-24 months old children will be included. [+7]

Exclusion criteria include psycho-neurological diseases, other sensorineural or...

Status: Not yet recruiting

Interest of Telemedicine in Primary Care in an Multidisability Population Institutionalized

Swallowing disorders are common and fall within the scope of primary care (as basic, essential health services accessible to all individuals within a community). These swallowing disorders, strongly linked to the environment, do not require, in the majority of cases, a technical and intrusive evaluation. The main objective of this project is to study the relevance of an assessment of dysphagia by teleconsultation

Participants needed: 62
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 28, 2026Locations: 5
Eligibility criteria

Patients aged ≥ 18 years living in a medical institution (MAS type, FAM from the... [+3]

Participation in another research including a period of exclusion still ongoing [+3]

Status: Not yet recruiting

Women Who Are Victims of Violence: Treatment of PTSD Through Reactivation of Traumatic Memories Using Propranolol

Post-traumatic stress disorder (PTSD) develops after life-threatening events, with domestic violence and sexual assault being major risk factors. An innovative approach using traumatic memory reactivation with propranolol has shown promise in reducing PTSD symptoms. This study aims to compare the efficacy of propranolol with trauma-focused psychotherapy in women suffering from severe PTSD after violence.

Participants needed: 70
Trial details
Phase: Phase 3Age: 18-75Biological sex: FemaleType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 28, 2026Locations: 2
Eligibility criteria

Women aged from 18 to 75 years [+5]

Systolic blood pressure below 100 mm Hg. [+20]

Status: Recruiting

Modelling of Pharyngeal Laryngeal Effectiveness

The purpose of this study is to collect the signals of pharyngeal laryngeal activity through five non-invasive sensors (microphone, accelerometer, surface electromyography (EMG), nasal cannula and oximeter) in order to identify indicators of functional efficiency of swallowing, protection of the lower airways and phonation. 440 patients (subjects with swallowing disorders), spread over 4 centers and 80 healthy subjects spread over 2 centers will be recruited for the study in an interventional research study involving the prospective, multicentric and longitudinal. Pharyngolaryngeal effectiveness will be measured from 6 indicators identified by examinations or reference tests grouped into 3 functions: * swallowing: pharyngeal transport capacity (Yale Residue) and Penetration Aspiration Scale (PAS) rated by videofluoroscopy of swallowing (VFS) or flexible endoscopic evaluation of swallowing (FEES); * airway protection: cough trigger (citric acid test) and cough power (peak expiratory flow); * phonation: vocal efficiency (maximum phonation time) and velar efficiency (nasal scores). The signals obtained from the 5 sensors will be annotated. Stochastic modelling based on hidden Markov models will be used initially and followed by the implementation of deep neural networks to model indicators. For the complication's prediction algorithm, deep neural networks will also be used to evaluate signal-based methods. The expected benefits are to obtain automated recognition of pharyngeal-laryngeal effectiveness to diagnose swallowing disorders using objective and quantifiable indicators, non-invasive devices, to assess the severity of these disorders and to identify the risk of complications.

Participants needed: 520
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 13, 2026Locations: 4
Eligibility criteria

Indication to perform a swallowing test (suspected or proven swallowing disorder... [+26]

Status: Not yet recruiting

Development and Validation of a Scale of Propensity for Change in Chronic Disease Prevention

Modifiable risk factors are estimated to account for 70% of cardiovascular diseases, 40% of Alzheimer's-type dementias, and 50% of type 2 diabetes cases. Numerous trials have evaluated interventions aimed at modifying these risk factors, whether through the promotion of healthy lifestyle choices (diet, physical activity, etc.) or specific activities (cognitive training, etc.). However, these trials have yielded inconsistent or modest results, potentially due to a failure to adopt the recommended lifestyle changes. To better tailor prevention interventions, it is therefore essential to have scales available that measure the barriers to and facilitators of lifestyle change. The aim of this study is to develop and validate a Patient-Reported Outcome Measure (PROM) to assess the barriers to and facilitators of change following participation in a prevention program. The scale will be structured into three sub-scales (capability, opportunity, and motivation), administered one month after the prevention activity, and will distinguish between the adoption of new habits and the abandonment of existing ones.

Participants needed: 290
Trial details
Age: 45+Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Aug 14, 2026Locations: 1
Eligibility criteria

Participant receiving a personalized prevention intervention through the frailty... [+2]

Participant unable to improve their lifestyle, according to the scales used in t... [+2]

Status: Not yet recruiting

Discontinuation or Continuation of SGLT-2 Inhibitors Before Cardiac Surgery

SGLT-2 inhibitors are recommended treatments for managing heart failure patients. In cases of surgery, it is recommended to stop the treatment 3 days before surgery due to the risk of postoperative euglycemic diabetic ketoacidosis. However, several data suggest that it may be beneficial to maintain SGLT-2i treatment given the possibility of improving postoperative cardiovascular outcomes. Investigator team wish to conduct a randomized controlled trial to test the hypothesis that preoperative maintenance of SGLT-2i is superior to discontinuing them 3 days before surgery in improving postoperative cardiovascular outcomes.

Participants needed: 434
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 14, 2026Locations: 1
Eligibility criteria

Adult patients scheduled to undergo cardiac surgery with cardiopulmonary bypass [+4]

Treatment with SGLT-2 inhibitors initiated less than 4 weeks ago and other than... [+11]

Status: Not yet recruiting

Study of Cognitive-Linguistic Profiles: The Role of Executive Control in Aphasia

In France, stroke affects 150,000 people annually and is the leading cause of acquired disability in adults; 10-12% of patients exhibit mild post-stroke aphasia, a condition defined by language difficulties. Few studies describe mild post-stroke aphasia, and none characterize the impairment of linguistic executive control in this population; consequently, its prevalence remains unknown. To date, the role of linguistic executive control in mild aphasia remains an open question. The aim of this project is to investigate linguistic executive control impairment in stroke survivors with mild aphasia, provide an initial estimate of its prevalence, and demonstrate its interactions with other linguistic and communicative aspects, as well as with executive and attentional functions.

Participants needed: 30
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 14, 2026Locations: 1
Eligibility criteria

Patient who has experienced a first ischemic stroke resulting in clinical sympto... [+3]

Patients exhibiting behavior or a clinical condition incompatible with test admi... [+3]

Status: Not yet recruiting

Analysis of the Performance of PSMA Emission Tomography in Patients With Prostate Cancer Treated With HIFU

There would appear to be a strong interest in functional nuclear imaging for assessing the response to focal PaC treatment. Investigator team hypothesise that the diagnostic performance of PSMA PET is noninferior to that of MRI in detecting clinically significant recurrent PaC after treatment with HIFU. The main objective was to evaluate the diagnostic performance of PSMA PET compared with MRI with reference to the gold standard of prostate biopsy one year after HIFU.

Participants needed: 30
Trial details
Phase: Phase 4Age: 70+Biological sex: MaleType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 14, 2026Locations: 1
Eligibility criteria

Patient with prostate cancer [+6]

Evidence of extra-prostatic extension or invasion of the seminal vesicles. [+7]

Status: Recruiting

Effect of Anomia Rehabilitation Combined With Metacognitive Training in Patients With Chronic Vascular Aphasia

The postulate of this study is that rehabilitation combining linguistic and metacognitive training will result in a significant improvement in language performance correlated with changes in functional cerebral connectivity networks. In addition, it could potentiate the generalisation of effects to verbal and non-verbal communication skills, having a direct impact on patients' quality of life. This research is a prospective, randomized controlled, open-label, single-centre study. It is part of the management of patients with aphasia who have suffered a cerebral infarction and aims to evaluate the effect of combined language semantics/metacognition rehabilitation.

Participants needed: 18
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 11, 2026Locations: 1
Eligibility criteria

First cerebral infarction [+4]

Contraindication to undergoing brain MRI [+5]

Status: Recruiting

Impact of Procalcitonin-guided Algorithm on Early Discontinuation of Antibiotic Therapy

In this randomized controlled open-label trial, conducted in 7 French Pediatric and Neonatal Intensive Care Units (ICUs), investigator team hypothesize that the use of a procalcitonin (PCT)-guided algorithm to discontinue antibiotic treatment will decrease antibiotic duration in critically ill children treated for a suspected or proven bacterial infection. Two hundred and ninety-six eligible patients will be randomly assigned in two groups: either PCT-guided or standard-of-care antibiotic discontinuation, and monitored over 28 days, until the end of their hospitalization, or up to the end of antibiotic treatment for bacterial infection recurrence occurring up to 28 days after the day of randomization.

Participants needed: 296
Trial details
Age: 3-17Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 11, 2026Locations: 8
Eligibility criteria

Neonates, infants and children hospitalized in Pediatric and Neonatal ICU and re... [+3]

Newborns <72 hours old. [+9]

Status: Recruiting

Physicians Performance After Night Shifts

Emergency medicine is one of the professional activities integrating a night activity into working time. Concerns about the sleep deprivation that this activity generates have been growing for the past thirty years. However, at present, the pace - duration and repetition - of this activity does not yet seem to be optimized, and therefore continues to be the subject of questions in terms of safety of care and quality of life at work. One of the peculiarities of emergency medicine is that doctors have to work in a crisis situation. A situation is qualified as critical for a patient when his state of health is unstable, and with an evolution which can be rapidly pejorative. Crisis situations are at the heart of the emergency room profession, and due to their potential seriousness for the patients, it must be managed in all circumstances. To cope with a crisis situation, a doctor needs to be efficient. However, performance calls for two types of skills: technical skills on one hand, and non-technical skills on the other. This study therefore aims to answer the following question: are the non-technical skills of emergency physicians in the management of a crisis situation affected twenty-four hours after the end of a night shift? The study assesses the performance of emergency physicians via complex simulations at two time frames : 24h after a night shift (the post recovery performance simulation) and another time were the participant did not have night shifts in less than 3 nights (usual performance simulation).

Participants needed: 40
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 11, 2026Locations: 1
Eligibility criteria

be an emergency doctor with an emergency medicine capacity, [+3]

non-emergency doctor [+2]

Status: Recruiting

Semantic Rehabilitation for Patients With Primary Progressive Semantic Aphasia

This project aims to measure the effect of a semantic rehabilitation protocol for patients with primary progressive semantic aphasia and using the SCED methodology.

Participants needed: 15
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 11, 2026Locations: 1
Eligibility criteria

Have a diagnosis of primary progressive semantic aphasia according to the criter... [+4]

Have significant uncorrected visual and/or hearing impairment [+6]

Status: Recruiting

Evolution of Balance and Vestibular Function in Patients Treated With Gammaknife Radiosurgery for Vestibular Schwannoma

Vestibular schwannomas are benign lesions of the ponto-cerebellar angle that are potentially dangerous because of their growth in a cramped space and the compressive phenomena they can cause. Stereotactic Gammaknife radiosurgery is a treatment option that can be offered for evolutive schwannomas smaller than 2.5-3 cm in size. It allows tumor stabilisation in 85% of cases with less than 1% facial nerve damage risk. There are controversial results regarding hearing preservation : percentages vary between 25 and 80% in the literature, depending on the criteria used and the post-treatment delay. Few studies have investigated changes in vestibular function and the impact on balance of radiosurgery, and their results are variable. These controversial results lead us to comprehensively assess the vestibular function and balance of these patients using a balance-specific quality of life questionnaire, in addition to objective overall vestibular assessments of vestibular function.

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 11, 2026Locations: 1
Eligibility criteria

Vestibular schwannoma's Patients for whom an indication of gammaknife radiosurge... [+2]

History of prior treatment for the presented vestibular schwannoma (surgery, fra... [+4]

Status: Recruiting

JAK Inhibitor Dose TAPering Strategy Study

This study aims to assess the feasibility of tapering JAK inhibitors in rheumatoid arthritis patients in low disease activity by comparing a group of patients tapering the JAK inhibitor dosage to a group of patients continuing the full-dose. Participants will: * Either take 1. JAK inhibitor dose-tapering strategy. 2. JAK inhibitor continuous therapy strategy. * Visit the clinic once every 3 months for checkups and tests * Keep a diary of their treatment intake and symptoms

Participants needed: 308
Trial details
Phase: Phase 4Age: 18-65Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 7, 2026Locations: 24
Eligibility criteria

Aged ≥ 18 years at baseline. [+23]