Clinical trials

286

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

Condition / disease
Location
Status: Not yet recruiting

Effect of Gingival Mesenchymal Stem Cell-Derived Small Extracellular Vesicles in Management of Infra-bony Periodontal Defect

The goal of the study to evaluate whether the adjunctive use of gingival mesenchymal stem cell-derived extracellular vesicles (GMSC-derived EVs) combined with β-tricalcium phosphate (β-TCP) and a collagen membrane results in superior radiographic bone fill compared to β-TCP and collagen membrane alone in the surgical management of infra-bony periodontal defects over a 6-month follow-up period.

Participants needed: 22
Trial details
Phase: Phase 2Age: 20-40Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Oct 9, 2026Locations: 1
Eligibility criteria

Healthy Individuals [+6]

Status: Not yet recruiting

Role of Inhaled Polymyxin as an Adjunct to Intravenous Therapy in Multidrug Resistant Ventilator-associated Pneumonia in Stroke Patients

This study investigates whether adjunctive inhaled colistin enhances clinical recovery and microbiological clearance in multidrug resistant ventilator-associated pneumonia in stroke patients

Participants needed: 78
Trial details
Phase: Early Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Oct 8, 2026
Eligibility criteria

Patients with cultures sensitive to colistin will be excluded.

Status: Not yet recruiting

the Effect of Ginkgo Biloba on Rheumatoid Arthritis Patients

this study aims to measure The Effect of Gingko Biloba on the Clinical Outcome of Rheumatoid Arthritis Patients ,the outcomes are hsCRp,calprotectin,DAS-28,HAQ-DI

Participants needed: 50
Trial details
Phase: Phase 2, Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Oct 6, 2026
Eligibility criteria

Adult patients (older than 18 years) - [+2]

Patients with known hypersensitivity to Ginkgo biloba [+5]

Status: Not yet recruiting

Low-Volume Pericapsular Nerve Group (PENG) Block With Dexamethasone vs Standard-Volume PENG Block After Total Hip Arthroplasty

The goal of this clinical trial is to compare two regimens of the pericapsular nerve group (PENG) block, an ultrasound-guided injection of local anaesthetic targeting the nerves supplying the front of the hip joint, for postoperative pain relief and quadriceps muscle function in patients undergoing primary unilateral total hip arthroplasty under spinal anaesthesia. The PENG block was originally proposed as a motor-sparing technique. However, the standard 20 mL volume can spread to the femoral nerve and cause quadriceps weakness. Reducing the injected volume may limit this spread and better preserve quadriceps strength, but smaller volumes risk shorter analgesic duration. Adding dexamethasone to a low-volume injection may compensate for the reduced volume. The main questions this trial aims to answer are: * Does a low-volume PENG block (10 mL bupivacaine 0.25%) with 4 mg dexamethasone differ from a standard-volume PENG block (20 mL bupivacaine 0.25%) in the time to first rescue analgesia? * Does it differ in the incidence and severity of quadriceps weakness on the operated side? Researchers will compare: * Group A (standard-volume PENG block): 20 mL bupivacaine 0.25%. * Group B (low-volume PENG block with dexamethasone): 5 mL bupivacaine 0.5% plus 4 mL normal saline plus 4 mg dexamethasone in 1 mL, giving 10 mL of bupivacaine 0.25%. Participants will: * Receive spinal anaesthesia with heavy bupivacaine 0.5% and fentanyl. * Be randomly allocated to Group A or Group B using computer-generated random numbers. * Receive the PENG block under ultrasound guidance, performed by an anaesthesiologist expert in regional anaesthesia. * Receive intravenous paracetamol 1 g every 8 hours, with intravenous nalbuphine 5 mg as rescue analgesia when the pain score (NRS) is 4 or more. * Be assessed by an anaesthesiologist blinded to group allocation for pain scores at rest and on movement at 2, 6, 12 and 24 hours; quadriceps strength (MRC scale and straight leg raise) at 6, 12 and 24 hours compared with the preoperative baseline; total opioid consumption over the first 24 hours; and time to first ambulation within the first 24 hours. The primary outcome is the time from completion of the PENG block to the first administration of rescue analgesia, recorded over the first 24 hours postoperatively. The study will be conducted at Ain Shams University Hospitals (El Demerdash Hospital) and will include 60 patients (30 per group), aged 50 to 70 years, ASA physical status I or II.

Participants needed: 60
Trial details
Phase: Phase 4Age: 50-70Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Oct 5, 2026Locations: 1
Eligibility criteria

Physical status ASA I or II. [+3]

Patient refusal. [+8]

Status: Recruiting

"Osseodensification Efficacy on Molar Septum Expansion in Immediate Molar Implant Placement

The ideal positioning of immediate implants in molar extraction sockets often requires the osteotomy to be in the interradicular septum, which can be challenging in some cases, with traditional site preparation techniques. Also, the alveolar ridge undergoes various remodeling processes following tooth extraction, resulting in hard and soft tissue loss which complicates prosthodontic rehabilitation. Immediate implant placement help preserve the alveolar ridge dimensions and buccal ridge contour. While osseodensification has shown promise in enhancing primary stability and bone microarchitecture, its clinical and microstructural effects in molar extraction sockets remain underexplored. Although there is ample documentation of information on the temperature that is generated during preparation of implant sites, there are no studies available in the literature comparing conventional drilling and osseodensification techniques; therefore, the present investigation was aimed at analyzing the efficacy of osseodensification compared to conventional drilling in terms of bone dimensions preservation , changes in bone architecture during implant site preparation and heat generation to define which technique can be safely applied to achieve the necessary implant primary stability without damaging the surrounding bone. Aim of the study: Is to compare the molar septum dimensions using osseodensification expansion versus the conventional drilling protocol and to assess the role of jumping gap grafting in preservation of the alveolar ridge dimensions and buccal ridge contour in addition to Evaluation of the effect of osseodensification on the bony micro-architecture and heat generation

Participants needed: 80
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Oct 5, 2026Locations: 2
Eligibility criteria

Patients requiring placement in the posterior region. [+5]

Pregnancy. [+4]

Status: Recruiting

Safety and Efficacy of Papillary Versus NonPapillary Access During Percutaneous Nephrolithotomy

This study aims to evaluate and compare the safety, efficacy, and clinical outcomes of papillary and non-papillary renal access during percutaneous nephrolithotomy (PCNL), and to determine whether non-papillary puncture can be considered a safe and effective alternative to the conventional papillary approach in selected patients.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Oct 2, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years [+2]

Bleeding diathesis or uncorrected coagulopathy [+4]

Status: Recruiting

Effect of Melatonin on Pulmonary Hypertension in Full Term Neonates

The aim of the study 1. To evaluate safety and efficacy of melatonin as an adjuvant therapy to inhaled nitric oxide generated by NO generator in the treatment of pulmonary hypertension in full term neonates. 2. To assess the effect of inhaled nitric oxide and melatonin on cerebral perfusion.

Participants needed: 52
Trial details
Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Sep 30, 2026Locations: 1
Eligibility criteria

Term neonates with gestational age ≥ 37 weeks. [+1]

Congenital methemoglobinemia. [+3]

Status: Recruiting

Tetanus Severity Score for Prediction of Mortality in Manifest Tetanus

Three scoring systems will be applied to patients suffering from manifest tetanus and will be related to mortality.

Participants needed: 115
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

Adults (age 18 years old or more). [+3]

Age < 18 years. [+3]

Status: Recruiting

2D:4D Ratio in Relation to Anxiety and Stress Among Anesthesiology Residents

Anesthesiologists are exposed to substantial occupational stress, making their psychological well-being essential for both personal health and optimal patient care. Early identification of mental health disorders among healthcare professionals is important for improving well-being and maintaining healthcare quality.

Participants needed: 116
Trial details
Age: 20-35Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 30, 2026Locations: 1
Eligibility criteria

Any anesthesiologists who voluntarily agreed to participate in the study. [+2]

Incomplete questionnaires and/or irrelevant responses. [+5]

Status: Not yet recruiting

PCO₂ Gap and Lactate as Predictors of POCD After Cardiac Surgery

This prospective observational study aims to evaluate whether intraoperative venous-to-arterial carbon dioxide partial pressure difference (PCO₂ gap) and arterial lactate levels can serve as early predictors of postoperative cognitive dysfunction (POCD) in elderly patients undergoing elective cardiac surgery with cardiopulmonary bypass. Intraoperative measurements of PCO₂ gap and lactate will be correlated with perioperative cognitive outcomes assessed using the Montreal Cognitive Assessment (MoCA) and postoperative delirium screening using the Confusion Assessment Method for the ICU (CAM-ICU).

Participants needed: 185
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 25, 2026
Eligibility criteria

Age ≥65 years. [+3]

Refusal or inability to provide written informed consent. [+9]

Status: Recruiting

Chronic Unilateral Lumbar Radicular Pain

Chronic neuropathic lumbar pain is among one of the most widespread complaints of patients.Many approaches have been attempted to target chronic pain, with varying efficacy and risks. Transgrade (TG) epidural injection is a new technique using a Racz- Coudé needle for epidural access at a "transgrade" angle without requiring any specialized hardware or accessories. Interlaminar (IL) epidural steroid injection (ESI) is one of the procedures that involves the delivery of injectate to the epidural space through directing a needle between the laminae of two adjacent vertebrae.

Participants needed: 80
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Sep 24, 2026Locations: 1
Eligibility criteria

> 6-month history of persistent pain in one leg with back pain. [+2]

Previous lumbar spinal surgery. [+4]

Status: Recruiting

Preoperative Coadministration of Low-concentration Carbohydrate and Nitrates Loading vs Low- Concentration Carbohydrate Loading Alone in Patients Undergoing Open Gynecological Surgeries

Surgery is known to be associated with stress response affecting in a negative way the clinical outcome and patient experience. The stress response includes both sympathetic nervous system activation and systemic inflammatory response. The pituitary- sympathetic one leads to a number of metabolic changes as hyperglycemia, nitrogen loss and lipolysis on the other hand the systemic inflammatory response aggravates the perioperative metabolic changes. One of components of ERAS is preoperative carbohydrate load. Oral carbohydrate was associated with attenuation of the postoperative metabolic stress response. Nitrate rich drinks before exercises have a promising impact due to improving blood flow, mitochondrial efficiency, glucose uptake and the sarcoplasmic calcium handling all of which maximize resistance to fatigue and improved exercise performance.

Participants needed: 90
Trial details
Phase: Phase 4Age: 18-60Biological sex: FemaleType: InterventionalSponsor: Ain Shams UniversityUpdated: Sep 24, 2026Locations: 1
Eligibility criteria

Patients ageing from 18 to 60 years, [+2]

Previous chemotherapy treatment, [+7]

Status: Not yet recruiting

Automated vs Manual Polysomnography Scoring in Adults With Obstructive Sleep Apnea

This prospective study aims to compare automated polysomnographic scoring with manual scoring in adult patients with Obstructive Sleep Apnea (OSA). The main objective is to evaluate the accuracy, reliability, and time efficiency of automated scoring algorithms compared to standard manual scoring performed by expert sleep specialists

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 23, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Age > 18 years. [+2]

Age ≤ 18 years. [+3]

Status: Not yet recruiting

Nano Silver Fluoride and Photobiomodulation Therapy for Hypersensitivity and Pain in MIH-Affected Molars

Molar-incisor hypomineralization (MIH) is a developmental condition affecting primarily the first permanent molars and may be associated with post-eruptive enamel breakdown, hypersensitivity, and difficulties in achieving adequate pain control during dental treatment. This randomized controlled trial will evaluate the effectiveness of nano silver fluoride (NSF) and photobiomodulation therapy (PBMT) as desensitizing interventions applied before cavity preparation in children aged 7-12 years with MIH-affected first permanent molars with post-eruptive enamel breakdown. The study will compare the effects of NSF and PBMT with a control group receiving pre-appointment analgesics. Hypersensitivity will be assessed using the Cumulative Hypersensitivity Index (CHI), while pain during cavity preparation and restoration will be evaluated using the Wong-Baker FACES Pain Rating Scale and pulse rate monitoring. All treated molars will receive glass ionomer cement restorations, which will subsequently be evaluated using the Modified United States Public Health Service (USPHS) criteria at 3, 6, and 12 months.

Participants needed: 45
Trial details
Age: 7-12Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Sep 17, 2026
Eligibility criteria

Children aged 7-12 years diagnosed with molar-incisor hypomineralization (MIH) i... [+3]

Hypomineralized molars caused by other conditions, including syndromes, fluorosi... [+5]

Status: Recruiting

The Effect of Nicorandil on Rheumatoid Arthritis Patients

The aim of this clinical trial is to determine whether nicorandil works in minimizing disease severity in patients with rheumatoid arthritis. The study will also assess the safety and tolerability of nicorandil. The main questions it aims to answer are: * Could nicorandil improve disease severity and symptoms of rheumatoid arthritis? * Does nicorandil lower the number of times participants need to use pain relieve medications? * Does the nicorandil improve participants functionality and ability to carry out daily activity? * Does nicorandil correct disease-associated damage and inflammation? * What side effects do participants have when taking nicorandil? Researchers will compare nicorandil to a placebo (a look-alike substance that contains no drug) to see if nicorandil works to decrease symptoms and severity of rheumatoid arthritis. Participants will: * Take nicorandil or a placebo two times daily for 3 months * Visit the clinic once every month for checkups * Keep a diary of their symptoms and the number of times they use a pain reliever

Participants needed: 70
Trial details
Phase: Phase 2, Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Sep 16, 2026Locations: 1
Eligibility criteria

Adult (≥18 years). [+4]

Other autoimmune diseases [+9]

Status: Recruiting

Palmitoylethanolamide in Ulcerative Colitis

Evaluate the effects of PEA supplementation on disease activity, health-related quality of life (HRQoL) and inflammatory biomarkers in patients with active mild-to-moderate UC.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Sep 15, 2026Locations: 1
Eligibility criteria

Confirmed diagnosis of ulcerative colitis (UC) by established clinical and endos... [+1]

Pregnancy or breastfeeding. [+12]

Status: Not yet recruiting

SV and IVC Collapsibility Index to Predict Postinduction Hypotension

Postinduction hypotension (PIH) is a frequent complication during general anesthesia. This study aims to compare the predictive effectiveness and diagnostic accuracy of stroke volume (SV) measured via left ventricular outflow tract velocity time integral (LVOT-VTI) versus the inferior vena cava collapsibility index (IVC-CI) using transthoracic echocardiography. The assessment will be conducted in adult patients with intestinal obstruction undergoing exploratory abdominal surgery under general anesthesia.

Participants needed: 75
Trial details
Age: 40-70Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 10, 2026
Eligibility criteria

Adult patients with intestinal bowel obstruction undergoing exploratory abdomina... [+3]

American Society of Anesthesiologists (ASA) physical status grade >= III. [+5]

Status: Recruiting

Oral Verapamil Among Newly Diagnosed Children and Adolescents With Type 1 Diabetes

Type 1 diabetes (T1D) in children involves autoimmune destruction of pancreatic ß- cells, leading to insulin deficiency. Verapamil is an L-type calcium channel blocker that has been used for decades to treat hypertension and certain cardiac conditions. Recent research has revealed its potential as a ß- cell-protective agent. Hence this study will evaluate the effect of once-daily oral verapamil on pancreatic ß- cell reserve , glycemic metrics and daily insulin requirements in children and adolescents with T1D.

Participants needed: 70
Trial details
Phase: Phase 2, Phase 3Age: 10-18Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Sep 4, 2026Locations: 1
Eligibility criteria

Children and adolescents aged 10-18 years. [+3]

Previous diagnosis of other endocrine disorders or autoimmune disorder (e.g. aut... [+8]

Status: Recruiting

Effect of Intravenous Magnesium on Postoperative Systemic Inflammatory Response in Patients Undergoing Colorectal Cancer Surgery

The aim of this study is to detect the effect of intraoperative intravenous magnesium sulfate on postoperative systemic inflammatory response by serum inflammatory parameters as CRP, WBCS and neutrophil count.

Participants needed: 52
Trial details
Age: 35-75Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Sep 3, 2026Locations: 1
Eligibility criteria

ASA I and ASA II. [+3]

Renal impairment (Glomerular Filtration Rate < 60 ml\min). [+10]

Status: Recruiting

Ultrasound Detection of Body Composition in Critical Care

Objective assessment of the Changes in body composition of critically ill patients is very valuable. Ultrasound stands as a solution due to its portability, bedside availability, and radiation-free technology. Those criteria are crucial for critically ill obstetrics and gynecological cases.

Participants needed: 121
Trial details
Age: 16+Biological sex: FemaleType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 4, 2026Locations: 1
Eligibility criteria

females with age 16 with no upper limit [+2]

Patient refusal

Status: Recruiting

Establishing a National Egyptian HLH Registry (NEHR)

Establishing a National Egyptian HLH Registry (NEHR)

Participants needed: 100
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 2, 2026Locations: 2
Eligibility criteria

patients diagnosed with hlh

adults

Status: Recruiting

Hemoglobin Disorders in Egypt: Sickle Cell Disease Ain Shams University Institutional Registry

This is a retrospective descriptive study to create an institutional registry that will continue as a prospective follow-up non-intervention study that will be carried out at Hematology Oncology and BMT Department, Children's Hospital, Ain-Shams University, Cairo, Egypt.

Participants needed: 400
Trial details
Age: Up to 39Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 2, 2026Locations: 2Duration: 2 Years
Eligibility criteria

children, adolescents and young adults with sickle cell disease

other inherited anemia

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 1, 2026
Eligibility criteria

Adult patients aged ≥ 18 years with septic shock. [+2]

Patient <18 years. [+4]

Status: Recruiting

Efficacy of Multiple Nerve Blocks on the Recovery of Patients Undergoing Off Pump CABG Surgeries

In cardiac surgery patients , effective pain control is crucial to support early extubation, mobilization, and cognitive recovery, yet systemic opioids carry substantial risks such as respiratory depression, delirium, and delayed rehabilitation. While regional fascial plane blocks offer a safer, opioid-sparing alternative, no single technique provides complete analgesia for the complex and multi-dermatomal pain generated by sternotomy, graft harvesting, chest wall retraction, and drain sites. Therefore, a multimodal approach combining blocks such as parasternal nerve block , rectus sheath nerve block and femoral nerve block , may cover most of areas expected to be sources of intraoperative and post-operative pain in cardiac surgery patients.

Participants needed: 30
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Aug 31, 2026Locations: 1
Eligibility criteria

o Scheduled for elective off-pump coronary artery bypass graft (OPCAB) surgery v... [+2]

o Emergency or redo cardiac surgery [+9]

Status: Recruiting

Red Cell Distribution Width/Albumin Ratio as a Predictive Tool for Mortality of Patients With Burn Injuries

The aim of this study is to evaluate the prognostic utility of the red cell distribution width/albumin ratio (RAR), measured within 24 hours of hospital admission, in predicting 30-day mortality among patients with burn injuries.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Aug 18, 2026Locations: 1Duration: 30 Days
Eligibility criteria

Age > 18 years. [+4]

Age <18 years. [+7]