Clinical trials

1,095

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

Condition / disease
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Status: Not yet recruiting

Hyaluronic Acid and Polynucleotides With Connective Tissue Graft and Coronally Advanced Flap for RT II Gingival Recession

This case series will evaluate the effectiveness of injectable hyaluronic acid combined with polynucleotides as an adjunct to coronally advanced flap and connective tissue graft in patients with RT II gingival recession. Twelve patients will be included and followed for 6 months. Clinical outcomes will include percentage of root coverage, clinical attachment level gain, gingival thickness, probing depth, width of keratinized tissue, post-operative pain, and patient aesthetic satisfaction.

Participants needed: 12
Trial details
Age: 15-60Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 21, 2026Locations: 1
Eligibility criteria

Patients with RT II gingival recession. [+3]

Periodontitis. [+4]

Status: Recruiting

Bariatric Endoscopic Antral Myotomy Combined With Fundal Gastric Mucosal Ablation

The gastric fundus regulates appetite through orexigenic ghrelin-mediated and anorexigenic visceroceptive pathways. Accordingly, endoscopic gastric fundal mucosal ablation (GFMA) may benefit patients with obesity. Ablation not only affects these mechanisms, but similar to what happens after mucosal ablation for other indications (e.g. ESD for tumor removal), it is expected to cause shrinking of the fundus and reduce gastric volume. Another potential target to achieve weight loss is gastric emptying. This is a critical step in digestion that has been found to be more rapid after prolonged exposure to a high-fat diet in both animal and human studies, with rapid emptying also being more common in young people with obesity in some studies. The bariatric endoscopic antral myotomy (BEAM) procedure has been shown to consistently delay gastric emptying without triggering symptoms of gastroparesis and to produce substantial weight loss. Both GFMA and BEAM procedures have the advantages of being minimally invasive, performed completely endoscopic and less costly than surgical alternatives or other known endoscopic techniques like intragastric balloon or endoscopic sleeve gastroplasty.

Participants needed: 10
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 21, 2026Locations: 1
Eligibility criteria

Subjects with any previous surgeries to the stomach [+5]

Status: Recruiting

Electromyographic Effects of Postural Correction Exercises in Individuals With Forward Head Posture

This study investigates the effects of specific corrective exercises on EMG of masticatory and cervical muscles in individuals with forward head posture. The study's design will be a retrospective, double- blinded, randomized controlled trial. The participants will be randomly allocated to one of two groups: the exercise group and the control group. The training groups will perform a program consisting of two strengthening (deep cervical flexors and shoulder retractors) and two stretchings (cervical extensors and pectoral muscles) exercises. This exercise program will be repeated 4 times per week for 10 weeks, and each session lasted 30 minutes. The pre/post assessment of forward head posture will measure by using craniovertebral angle CVA. While the muscle activity EMG of the masseter, temporalis, splenius, upper trapezius, and SCM will measure pre and post-assessment using a biopic data acquisition system.

Participants needed: 60
Trial details
Age: 18-30Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 21, 2026Locations: 1
Eligibility criteria

1. Participants aged 18- 30 years. 2. Presence of forward head posture, defined...

1. Current or previous diagnosis of temporomandibular disorder (TMD), or the pre...

Status: Not yet recruiting

Effect of Probiotic on Cognitive Function

The goal of this clinical trial is to learn if daily single-strain probiotic supplementation (Lactobacillus plantarum) works to improve cognitive function and depressive symptoms in Egyptian women aged 50-64 years with mild depression. It will also learn about its effects on systemic inflammation and autonomic nervous system function via the gut-brain axis The main questions it aims to answer are: Does a 12-week probiotic supplementation improve cognitive function (measured by MoCA-B) compared to a placebo? Does it reduce the severity of depressive symptoms (measured by BDI-II)? Does it reduce systemic inflammation (measured by hs-CRP levels in the blood)? Does it enhance autonomic nervous system function (measured by Heart Rate Variability - HRV via a smartphone app)? Researchers will compare the probiotic capsule (Lactobacillus plantarum, 10 billion CFU) to a placebo (a look-alike capsule containing starch) to see if the probiotic works better than placebo. Participants will: Take one probiotic or placebo capsule orally every morning with breakfast for 12 weeks. Visit the Family Medicine outpatient clinic at baseline and at 12 weeks for cognitive and psychological tests, HRV measurements, and blood tests. Receive weekly follow-up messages on WhatsApp to monitor adherence and report any dietary changes or potential side effects.

Participants needed: 88
Trial details
Age: 50-64Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Aug 20, 2026Locations: 1
Eligibility criteria

Presence of mild depressive symptoms, defined as a Beck Depression inventory II... [+1]

Moderate and severe depression (BDI-II score > 19) or active suicidal ideation (... [+9]

Status: Not yet recruiting

Transverse Perineal Support With STARR for Anterior Rectocele With Excessive Perineal Descent

This prospective randomized controlled trial will include adult patients with ODS, anterior rectocele ≥3 cm, and excessive perineal descent following failure of conservative treatment. Patients will be randomized 1:1 to STARR alone or STARR combined with transverse perineal support procedure using polypropylene mesh. The primary outcome will be Change in Altomare Obstructed Defecation Syndrome (ODS) score in both groups. Secondary outcomes will include operative time, postoperative pain, surgical complications, surgical site infection, and sexual function assessed using the PISQ-12. Patients will be followed up twice during the first postoperative week, weekly during the first month, and monthly thereafter.

Participants needed: 64
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 20, 2026Locations: 1
Eligibility criteria

Adult patients complaining of obstructed defecation syndrome with anterior recto...

Patients with Slow-transit constipation [+6]

Status: Not yet recruiting

Effects Of Otago Exercise Versus Multisensory Integration Training On Balance And Gait In Elderly With Diabetes

The goal of this clinical trial is to compare the effect of the Otago exercise and Multisensory integration training on balance and gait in the elderly with type 2 diabetes mellitus. The main question it aims to answer is: • Is there a significant difference between the effect of Otago exercise and Multisensory integration training on balance and gait in the elderly with type 2 diabetes mellitus? Researchers will compare Otago exercise to Multisensory integration training to know which one has the greatest benefit on balance \&gait in the elderly with type2 diabetes. Participants will be divided into 3 groups; each group takes a certain training program for 8 weeks: * First group: Otago exercise group plus conventional treatment for neuropathy. * Second group: Multisensory integration training group plus conventional treatment for neuropathy. * Third group: control group takes only conventional treatment for neuropathy.

Participants needed: 90
Trial details
Age: 65-75Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 20, 2026Locations: 1
Eligibility criteria

Ninety elderly Patients of both genders. [+8]

Any musculoskeletal disorder affecting the lower limb (fracture of the lower lim... [+9]

Status: Not yet recruiting

Clinical and Radiographic Success of Calcium Hydroxide-Iodoform Paste Versus Modified Triple Antibiotic Paste for Necrotic Primary Molars in Children

This randomized clinical trial aims to compare the clinical and radiographic success of calcium hydroxide-iodoform paste and modified triple antibiotic paste when used for the treatment of necrotic primary molars in children using the lesion sterilization and tissue repair (LSTR) technique. The study will include children aged 4-7 years with restorable necrotic mandibular second primary molars. Participants will be randomly assigned to receive LSTR treatment with either calcium hydroxide-iodoform paste or modified triple antibiotic paste. Clinical and radiographic findings will be assessed during follow-up over 12 months to determine the success of each treatment. The study hypothesis is that there will be a difference in the clinical and radiographic success between the two treatment materials when used with the LSTR technique

Participants needed: 50
Trial details
Age: 4-7Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 19, 2026
Eligibility criteria

Pediatric patients aged 4-7 years [+3]

Medically compromised patient [+5]

Status: Not yet recruiting

Efficacy of AI-Driven and Traditional Physical Therapy Programs in Patients With Knee Osteoarthritis

This study aims to compare the effectiveness of an artificial intelligence (AI)-guided physical therapy program with a traditional physical therapy program in patients with knee osteoarthritis. Forty patients with knee osteoarthritis will be randomly assigned to one of two groups. The traditional physical therapy group will receive a conventional rehabilitation program including transcutaneous electrical nerve stimulation (TENS), strengthening, flexibility, and balance exercises. The AI-guided group will receive an individualized rehabilitation program generated using ChatGPT-4 based on standardized patient information and clinical assessment findings. Both groups will receive education regarding lifestyle modification and joint protection strategies. The effects of the two rehabilitation approaches will be evaluated by measuring pain intensity, knee range of motion, knee-related functional ability, and functional mobility and fall risk before and after the intervention. The study will determine whether an AI-guided physical therapy program can provide outcomes comparable or superior to those of traditional physical therapy in individuals with knee osteoarthritis.

Participants needed: 40
Trial details
Age: 45-70Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 19, 2026Locations: 1
Eligibility criteria

Participants will be recruited through outpatient orthopedic clinics and communi... [+4]

Prior knee replacement surgery, inflammatory arthritis (e.g., rheumatoid arthrit... [+3]

Status: Not yet recruiting

Polynucleotide-Hyaluronic Acid Gel With Xenograft for Alveolar Ridge Preservation

This randomized controlled clinical trial will evaluate the efficacy of polynucleotide-hyaluronic acid gel combined with xenograft and collagen membrane for alveolar ridge preservation following tooth extraction. Twenty participants will be randomly allocated into two parallel groups. The test group will receive xenograft mixed with polynucleotide-hyaluronic acid gel and covered with a collagen membrane, while the control group will receive xenograft with a collagen membrane alone. Clinical and CBCT assessments will be performed at baseline and during follow-up. After 6 months, ridge dimensional changes will be evaluated and core biopsies will be obtained at the time of implant placement for histological assessment.

Participants needed: 20
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 18, 2026Locations: 1
Eligibility criteria

Patients aged 18-60 years. [+5]

Use of drugs affecting wound healing. [+5]

Status: Not yet recruiting

Effect of Low Level Laser Therapy on Women With Obstructive Defecation Syndrome

Obstructive defecation syndrome (ODS) is a condition in which a person has difficulty completely emptying the rectum during bowel movements. Women with ODS may experience excessive straining, a feeling of incomplete evacuation or blockage, abdominal discomfort, and the need to use manual assistance, laxatives, or enemas to facilitate defecation. This randomized controlled trial will investigate the effect of adding low-level laser therapy (LLLT) to a conventional treatment program for women with ODS. Participants will be randomly assigned to one of two groups. The control group will receive nutritional modification and biofeedback training, while the study group will receive the same treatment in addition to low-level laser therapy applied to the lumbosacral region. The study will evaluate whether adding low-level laser therapy can improve anorectal function, reduce the severity of ODS symptoms, and improve health-related quality of life compared with conventional treatment alone.

Participants needed: 40
Trial details
Age: 30-45Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Aug 18, 2026Locations: 1
Eligibility criteria

Woman diagnosed with ODS according to the Renzi ODS score (≥ 9). [+4]

Any abnormalities around cancer colon, interstitial cystitis, or endometriosis. [+5]

Status: Not yet recruiting

Effect of Prophylaxis Pastes With and Without Desensitizing Agents Prior to In-office Bleaching

To evaluate the effect of prophylaxis pastes with and without desensitizing agents prior to in-office bleaching on color change and tooth sensitivity.

Participants needed: 38
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 18, 2026
Eligibility criteria

Patients who have discolored teeth, minimum of 20 natural teeth, good oral hygie...

Patients who have extensive prosthesis or restoration, tetracycline discoloratio...

Status: Not yet recruiting

Fine Motor Performance in School-aged Children

The goal of this observational cross-sectional study is to investigate the relationship between core stability, hand grip strength, and handwriting performance in typically developing school-aged children aged 8 to 12 years. The study aims to determine whether core stability is associated with upper extremity function and handwriting abilities during middle childhood. The main questions the study aims to answer are: * Is there a relationship between core stability and hand grip strength in typically developing school-aged children? * Is there a relationship between core stability and handwriting performance in typically developing school-aged children? Participants will undergo the following assessments: * Assessment of core stability using the McGill core endurance tests. * Measurement of hand grip strength using a hydraulic hand dynamometer.

Participants needed: 100
Trial details
Age: 8-12Biological sex: AllType: ObservationalSponsor: Cairo UniversityUpdated: Aug 17, 2026
Eligibility criteria

Typically developing children aged 8-12 years. [+7]

History of neurological, developmental, or musculoskeletal disorders affecting p... [+4]

Status: Recruiting

Evaluating AI for Diagnosing and Treating Gummy Smiles: A Pilot Study

Some people have a "gummy smile," where too much gum tissue shows when they smile. Doctors currently diagnose this by hand, using rulers and visual judgment. This study is testing whether a computer program using artificial intelligence (AI) can help identify and measure gummy smiles from photographs, as accurately as expert dentists do it manually. Patients seen at Cairo University's Periodontics and Orthodontics clinics will have photos of their smile taken. Researchers will use these photos to first "teach" the AI program how to recognize and measure a gummy smile. Then, the AI will be tested on a new set of patient photos, and its measurements will be compared to measurements made by expert dentists, to see how closely they match. The goal is to find out whether this AI tool could one day help doctors diagnose gummy smiles more quickly and consistently, which may improve care for patients.

Participants needed: 210
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Cairo UniversityUpdated: Aug 12, 2026Locations: 1
Eligibility criteria

Properly treated gummy smile cases either surgical through crown lengthening pro...

Improperly treated gummy smile cases

Status: Not yet recruiting

Impact of Tibial Nerve Stimulation on Lumbopelvic Mechanics and Sexual Function in Females With Sexual Dysfunctions

This study will be conducted to examine the effects of Transcutaneous Tibial Nerve Stimulation (TTNS) on lumbopelvic mechanics and sexual function in females with sexual dysfunctions and low back pain

Participants needed: 40
Trial details
Age: 25-35Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Aug 14, 2026Locations: 1
Eligibility criteria

Females are diagnosed with low back pain combined with female sexual dysfunction... [+4]

Prior history of disc prolapse and sacroiliac joints, symphysis pubic joint as w... [+5]

Status: Not yet recruiting

Clinical and Radiographic Evaluation of Subgingival 1% Metformin Gel Versus 0.05% Zoledronate Gel as an Adjunct to MINST of Intrabony Defects in Controlled Type 2 DM

The present randomized placebo-controlled trial aims to evaluate and compare the clinical and radiographic efficacy of subgingivally delivered 0.05% zoledronate gel and 1% metformin gel as adjuncts to minimally invasive nonsurgical treatment of intrabony defects in patients with controlled type 2 diabetes mellitus and periodontitis.

Participants needed: 30
Trial details
Age: 30-60Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 11, 2026
Eligibility criteria

Diagnosed with type 2 diabetes mellitus, with HbA1c levels <7.0% (controlled). [+2]

Smokers. [+4]

Status: Not yet recruiting

Effect of Artificial Intelligence Based Cognitive Training on Sleep Disorders and Quality of Life in Patients With Multiple Sclerosis

this study will be conducted to investigate the effect of artificial intelligence (AI) based cognitive training on sleep disorders and quality of life in patients with multiple sclerosis.

Participants needed: 40
Trial details
Age: 25-40Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 13, 2026
Eligibility criteria

Patient's age ranges from 25-40 years. [+4]

Mechanical or neuromascular problems. [+3]

Status: Not yet recruiting

Aquatic Versus Land-Based Exercise in Women With Lipedema

To evaluate optimal workout environments, a 12-week study assigned women with moderate-to-severe lipedema to three distinct protocols: supervised pool workouts, equivalent land-based training, or basic standard monitoring. Researchers tracked walking endurance alongside tissue composition, fluid levels, pain intensity, and general well-being. The trial posited that structured activity beats routine care alone, with water-based exercise potentially offering superior relief due to buoyancy and hydrostatic fluid compression.

Participants needed: 60
Trial details
Age: 35-45Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Aug 11, 2026
Eligibility criteria

Women diagnosed with lipedema for at least five years [+5]

Had clinically significant lymphedema, uncontrolled chronic venous insufficiency... [+4]

Status: Not yet recruiting

Calisthenics Versus Cycling Exercises on Interleukin-6 and Quality of Life in Benha University Students With Irritable Bowel Syndrome

this study will be conducted to compare between the effect of calisthenics versus cycling exercises on interleukin-6 and quality of life in Benha University students with irritable bowel syndrome.

Participants needed: 60
Trial details
Age: 18-25Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Aug 12, 2026
Eligibility criteria

females will be aged from 18 to 25 years old [+3]

organic gastro -intestinal disorders [+9]

Status: Not yet recruiting

Core-Based Movement and Nutritional Counselling for Stress and Metabolic Outcomes in Overweight Women With Functional Constipation

This study will investigate the effect of core-based movement and nutritional counselling on stress, serum cortisol, and lipid profile in overweight women with functional constipation. Sixty overweight women with functional constipation will be randomly assigned into two equal groups. The study group will include 30 participants who will receive a core-based movement exercise program for 8 weeks, two sessions per week, in addition to guideline-based nutritional counselling. The control group will include 30 participants who will receive guideline-based nutritional counselling only for 8 weeks. The outcomes will include perceived stress, serum cortisol level, lipid profile, stool form, sleep quality, and quality of life.

Participants needed: 60
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Aug 10, 2026Locations: 1
Eligibility criteria

Female participants diagnosed with functional constipation according to Rome IV... [+4]

Participants will be excluded if they have any organic gastrointestinal disorder... [+7]

Status: Not yet recruiting

EFFICACY OF ARTIFICIAL INTELLIGENCE DRIVEN PROGRAM VERSUS TRADITIONAL PHYSICAL THERAPY PROGRAM IN PATIENTS WITH LOW BACK DYSFUNCTION

Low back dysfunction is one of the most common musculoskeletal disorders and is associated with pain, disability, and reduced quality of life. Artificial intelligence (AI) has emerged as a promising tool to support personalized rehabilitation by improving exercise prescription, monitoring adherence, and providing real-time feedback. This randomized controlled trial aims to compare the effectiveness of an AI-driven rehabilitation program with a traditional physical therapy program in patients with low back dysfunction. Primary outcomes include pain intensity, functional disability, and quality of life. The findings may provide evidence regarding the role of AI-assisted rehabilitation in improving clinical outcomes.

Participants needed: 68
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 7, 2026Locations: 1
Eligibility criteria

Adults aged 18-45 years. [+5]

Recent spinal injury or spinal surgery. [+6]

Status: Not yet recruiting

Diaphragmatic and Box Breathing on Heart Rate Variability and Perceived Stress

The goal of this clinical trial is to learn if diaphragmatic breathing and box breathing work to enhance resilience and manage stress in physical therapy students. It will also learn about their effects on overall physiological and psychological parameters. The main questions it aims to answer are: Do these breathing techniques improve heart rate variability (HRV)? How do these interventions affect participants' perceived stress levels, cognitive performance, and academic achievement? Researchers will compare diaphragmatic breathing and box breathing to a control group to see if these non-invasive methods work to improve physiological adaptation and manage stress. Participants will: Be randomly assigned to practice diaphragmatic breathing, practice box breathing, or join a control group Have their heart rate variability (HRV) measured as a primary sign of physiological adaptation Complete assessments to evaluate their perceived stress, cognitive performance, and academic achievement

Participants needed: 60
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 6, 2026Locations: 1
Eligibility criteria

Academic Status: Currently enrolled, full-time undergraduate Physical Therapy st... [+4]

Pre-existing Breathing Expertise: Individuals with professional training in yoga... [+7]

Status: Not yet recruiting

Effect of Transcranial Alternating Current Stimulation on Sleep Disorder and Anxiety in Elderly Population

Sleep disorders and anxiety are complicated disorders affecting population especially elderly population, therefore treating these disorders will have positive impact on population production and quality of life.

Participants needed: 60
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 7, 2026Locations: 1
Eligibility criteria

neurological and vascular diseases.

Status: Not yet recruiting

The Value of Pretreatment With Letrozole on Induction Time of Medical Evacuation With Misoprostol in Cases of Missed Abortion

The aim is to evaluate the effect of letrozole pretreatment on the induction time during medical evacuation using misoprostol in women diagnosed with missed abortion, and to compare its efficacy and safety to misoprostol alone.

Participants needed: 74
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Aug 7, 2026
Eligibility criteria

Women aged 18 - 45 years. [+5]

Incomplete abortion, inevitable abortion, or threatened miscarriage. [+7]

Status: Recruiting

Intermittent Ephedrine Boluses for Prophylaxis Against Postinduction Hypotension

The aim of this work is to assess the efficacy of intermittent ephedrine boluses in prophylaxis against postinduction hypotension in high-risk patients undergoing major abdominal surgery, compared to standard care.

Participants needed: 124
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Aug 6, 2026Locations: 1
Eligibility criteria

Adult patients aged >50 years, [+3]

Severe cardiac morbidities (impaired contractility with ejection fraction < 40%,... [+6]