Clinical trials

179

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Condition / disease
Location
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]

Status: Recruiting

Cognitive Remediation of Working Memory Post Head Trauma

Patients with working memory deficits due to a moderate to severe head injury will undergo a 5 month protocol including cognitive remediation with numerous exercises, transcranial direct current stimulation (tDCS), and therapeutic education.

Participants needed: 9
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Aug 7, 2026Locations: 1
Eligibility criteria

Moderate or severe head trauma, defined by an initial Glasgow score ≤ 12/15, dur... [+3]

Presence of aphasia, apraxia or severe neglect demonstrated by standardized neur... [+8]

Status: Not yet recruiting

Endoscopic Treatment

The placement of an endoprosthesis in the airways leads to rapid and dramatic clinical improvement in the majority of cases of central airway obstruction. However, the limited diversity of device shapes available on the market is a major limitation, as these devices are poorly adapted, or not adapted at all, to the patient's anatomy. The main consequences of this lack of congruity are stent migration and granulomatous inflammatory reactions. The investigators hypothesized that personalized endoprostheses could significantly reduce the complication rate and improve tolerability. In this randomized controlled trial, the investigators propose to evaluate whether personalized endoprostheses allow for better management of non-malignant central airway stenoses by comparing this new approach to standard care.

Participants needed: 96
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jul 27, 2026Locations: 6
Eligibility criteria

Age >18 years, [+4]

Acute respiratory distress, [+7]

Status: Recruiting

Predictive Factors for Occlusal Changes in Obstructive Sleep Apnea Treatment With Mandibular Advancement Appliance

This research addresses obstructive sleep apnea syndrome (OSAS), affecting 6-12% of French adults, often treated with mandibular advancement devices (MADs). MADs may lead to occlusal modifications, causing a 50% treatment abandonment rate. The study employs surface electromyography to assess masticatory muscle activity before and during MAD use, correlating it with occlusal changes after 6 months. The primary goal is to determine dental displacement profiles post-6-month MAD treatment, providing insights for personalized care and minimizing treatment failures.

Participants needed: 118
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Jul 23, 2026Locations: 1
Eligibility criteria

Patient with complete dentition (up to second molars) [+6]

Inability to provide informed consent [+2]

Status: Not yet recruiting

Evaluation of Botulinum TOXin Type A in the Treatment of Buerger's Disease

The main objective is to assess the feasibility of treatment by injecting botulinum toxin A into the hand or foot of patients with signs of critical ischemia secondary to Buerger's disease. The injection of botulinum toxin A is carried out at the end of a single session during an hospitalization. Furthermore, tolerance and effects on the disease are evaluated at 1, 3 and 6 months post injections.

Participants needed: 8
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jul 23, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years [+6]

History of myasthenia gravis or Eaton-Lambert syndrome [+13]

Status: Recruiting

Biomarkers of the Locus Coeruleus Nucleus: Links With Early Tau Pathology, Cognition and Alzheimer's Disease Risk

Alzheimer's disease (AD) is characterized by a long-lasting silent phase. Among initial events, emergence of tau pathology in locus coeruleus (LC) brainstem nucleus, well before the one observed in medial temporal cortex, is highly relevant. LC integrity and function can be assessed in vivo with MRI and pupil measures. The current research proposes to evaluate these LC markers in an aged healthy cohort (n=100, with half APOE4 positive) and to relate these markers with cerebral tau pathology, AD risk and cognitive function.

Participants needed: 100
Trial details
Phase: Phase 2Age: 60-100Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jul 17, 2026Locations: 1
Eligibility criteria

Participant in the INSPIRE-T cohort [+4]

Subjects with a contraindication to MRI exam [+4]

Status: Recruiting

Evaluation of a Cardiac Coherence Session to Reducing Patients' Anxiety During a MRI Examination

The present project aims at conducting a proof of concept study to explore the pertinence of a single session of cardiac coherence, carried out in patients prior to an MRI examination and presenting anxiety in relation to this examination, to reduce their level of anxiety and thus improve the course of the examination.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Jul 16, 2026Locations: 1
Eligibility criteria

Person affiliated to or benefiting from a social security scheme; [+8]

Status: Recruiting

Pilot Study: Home Use of Wearable Grasping Neuroprosthesis in Vascular Hemiparesis

Stroke is the leading cause of acquired motor disability in adults. Six months post-stroke, 50% of patients have not regained active finger extension, and 80% retain a grasping deficit, most commonly an inability to actively open the hand. This motor impairment significantly impacts daily activities, social interactions, professional life, and overall quality of life. Despite numerous treatments available in rehabilitation centers during the subacute phase, no functional assistive devices are currently usable at home. Since 2018, our team, in collaboration with the CAMIN-INRIA team, has developed a Grasp Neuroprosthesis (GNP). This device uses functional electrical stimulation to restore grasping function in hemiplegic subjects, enhancing autonomy in daily bimanual tasks. The GNP has been evaluated in hospital settings through two studies, defining preferred control modalities and demonstrating significant functional impact. Additionally, another study tested a wearable version of the GNP used autonomously at home for two months. This study showed the feasibility and functional benefits of home GNP use, provided the device is customizable to the patient's characteristics and environment. Initial results indicate improved quality of life and increased autonomy with GNP use. The wearable GNP consist of a forearm orthosis made of soft fabric, integrating an electrode array and a stimulator (CE medical marking for home use), connected via WiFi to a microprocessor positioned in a pouch. The microprocessor incorporates information from inertial measurement units and a microphone, allowing the user to control the electrical stimulator on demand. The stimulation targets the extensor muscles of the long fingers and the thumb, enabling the user to open the hand on demand. We propose extending the home use of the GNP to two patients for one year. Each subject will be followed for one year, with evaluations in a hospital setting at the beginning and end of the period, monthly follow-ups at home throughout the year, and on-demand video consultations.

Participants needed: 2
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 30, 2026Locations: 2
Eligibility criteria

Adult patient who participated in and completed the GRASP-AGAIN study and achiev... [+8]

The person is in labor or breastfeeding; [+17]

Status: Not yet recruiting

Biological Collection on Emerging Infectious Diseases and Their Treatments

Unprecedented changes in human-environment interactions and increasing disruptions to ecosystems and the climate have contributed to the emergence of infectious diseases (Emerging Infectious Diseases, EIDs). Advances in the treatment of cancers, malignant haematological disorders and immune-mediated inflammatory diseases are also contributing to the creation of new infectious risks among immunocompromised patient populations. The COVID-19 pandemic has shown that structuring research prior to any outbreak is essential for the rapid implementation of responses to the emergence of an EID. The unpredictability of an EID's occurrence necessitates the planning of research projects in advance. A key element in this planning is the development of a collection of biological samples, providing a structured and immediately deployable resource for conducting pathophysiological and therapeutic research aimed at: * Analyze the biological determinants of the microbe and the resulting infection * Develop new tools for identification and characterization * Study the factors (biomarkers/signatures) associated with individual patient susceptibility and response to treatment (personalized medicine) * Understand the pathophysiology of infection to identify new targets for diagnostic, curative and preventive treatment * Monitor the efficacy of curative and preventive treatments

Participants needed: 5,300
Trial details
Age: 18-99Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Jun 29, 2026Locations: 1Duration: 10 Years
Eligibility criteria

Patients aged 18 years or over [+4]

Status: Not yet recruiting

Platelets and Extracorporeal Membrane Oxygenation Veno-venous

In severe lung or heart disease, ExtraCorporeal Membrane Oxygenation (ECMO) may be used temporarily and can be responsible for major haemorrhagic complications. Thrombocytopenia and possibly thrombopathy promote bleeding. The primary objective is to characterize platelet dysfunction by aggregometry tests over time. Secondarily, investigators seek a correlation between haemorrhagic complications at day 10 and markers of platelet action and dysfunction; also, with the level of anticoagulation and inflammation by biomarkers.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Adults aged ≥ 18 years [+7]

Minors [+9]

Status: Recruiting

Combined Whole-brain Structural and Functional MRI for the Prediction of Neurological Recovery After Cardiac Arrest

To assess the performance of a predictive model resulting from the analysis of sMRI/fMRI/contrast-enhanced MRI-derived personalized connectomic data, as compared with standard predictors (clinical examination, electrophysiology, serum biomarker, standard neuroimaging) collected ≥ 72h from sedation withdrawal and in normothermia condition, to predict anoxoischemic coma neurological outcome at 6 months.

Participants needed: 263
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Adult patients (male or female ≥ 18 years). [+4]

Brain death. [+11]

Status: Not yet recruiting

Measuring the Evolution of Speech Perception in Noise, in Realistic Sound Environments According to Age

In clinical settings, hearing perception is typically assessed using audiometric tests administered in a controlled environment. To date, these tests are administered in silence or in the presence of noise from fixed sources at an arbitrarily predetermined signal-to-noise ratio. These assessment situations are not representative of the functional difficulties encountered by people with hearing loss or Auditory Processing Disorder in their daily lives. In real life, "soundscapes" are diverse. Hearing assessment and rehabilitation should include the child's everyday environments as well as their lifestyle habits. The Immersion 360 System (Virtual reality system) was developed specifically to virtually reproduce complex everyday sound experiences with realistic noise types and sound presentation conditions, enabling the assessment of auditory perception under test conditions similar to those encountered in daily life. Some of the sound environments offered by this innovative system have been standardized for adults. No standards exist for children, and we have limited knowledge regarding the development of speech perception skills in noise during childhood and adolescence. It seems essential to measure the age-related development of speech perception in realistic sound environments in order to establish reference data for children and adolescents. This work will, through functional assessments of the auditory system and linguistic tests (speech perception in noise), provide a better understanding of the functional development of the central auditory system for speech perception in noise. The results collected from normo-hearing individuals in the age groups of interest will provide a clinical baseline for comparison with patients of the same age.

Participants needed: 150
Trial details
Age: 7-15Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Children with normal hearing (average hearing thresholds at 250 Hz, 500 Hz, 1000... [+6]

Inability of the child to respond to tests [+9]

Status: Recruiting

Allogeneic Adipose Tissue Derived-stem Cells in Alzheimer Disease

A3D is a phase I/II clinical trial. The primary objective is to evaluate the safety of allogeneic adipose tissue derived-stem cells (AdMSC) administered by intravenous (IV) route in mild to moderate Alzheimer disease (AD) using a dose escalation protocol.

Participants needed: 9
Trial details
Phase: Phase 1, Phase 2Age: 50-85Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Patient between 50 and 85 years old [+5]

Brain disease (other than AD) that may cause dementia [+10]

Status: Recruiting

Radiofrequency Ablation Versus Adrenalectomy for Adenoma in Patients With Primary Aldosteronism and Hypertension

Primary aldosteronism (PA) is characterized by hypertension, frequent hypokalaemia, and an inappropriately high aldosterone-to-renin ratio (ARR). Aldosterone-producing adenoma (APA or Conn syndrome) is one of the main causes of primary aldosteronism. Laparoscopic (LA) total-adrenalectomy or adenoma selective is an option to normalize or at least improve blood pressure (BP) control, hypokalaemia, and normalize the ARR. However, the reported result of surgery is around 50% of clinical cure rate with an overall complication rate of 5 to 14% whereas hormonal success reached around 95%. More recently, radiofrequency ablation (RFA) has been used for patients with primary aldosteronism and unilateral adenoma. Investigator Team assume that treatment of unilateral PA by RFA could achieve similar efficacy to treatment by LA, with potentially less adverse events, and could be a more cost-efficient procedure.

Participants needed: 134
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 11, 2026Locations: 1
Eligibility criteria

Patient over 18 years of age [+9]

a negative lateralization of secretion on adrenal venous sampling [+19]