Clinical trials

202

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

Condition / disease
Location
Status: Recruiting

Detection of Early Scapular Dyskinesis

This study is a prospective blind contrast between periscapular muscle thickness measured with MSUS in patients with early AS in comparison to patients with mechanical dyskinesis and to correlate it with EMG findings.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Tanta UniversityUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

treatment-naïve patients with ankylosing spondylitis (AS), who fulfilled the Ass... [+1]

patients with a history of local trauma [+6]

Status: Recruiting

Microsurgical Single Versus Double Dartos Flap in Distal Hypospadias Repair

This study aims to compare the surgical and functional outcomes of microsurgical single dartos flap versus double dartos flap in distal hypospadias repair.

Participants needed: 100
Trial details
Age: 6-18Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Male patients diagnosed with Distal Hypospadias. [+4]

Coronal and glanular hypospadias. [+3]

Status: Recruiting

Intraarticular Injection of Botox and Hyaluronic Acid in Knee Osteoarthritis

This study aims to compare the efficacy of intra-articular injection of Botulinum toxin and hyaluronic acid on pain in knee osteoarthritis.

Participants needed: 50
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Age ≥ 50 years. [+3]

History of intra-articular injection within the last 6 months, [+6]

Status: Not yet recruiting

A Novel Suspensory Ligament Penodermal Fixation Technique Versus Dorsal Tunica Albuginea Fixation for Pediatric Buried Penis:

The aim of the work to compare the outcomes of suspensory ligament fixation to the sub-dermis and dorsal tunica albuginea fixation in terms of success rate, need for auxiliary procedures, and complication rates in the buried penis.

Participants needed: 40
Trial details
Age: 2-16Biological sex: MaleType: InterventionalSponsor: Tanta UniversityUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Children under the age of 18 years diagnosed [+1]

History of previous penile surgery. [+4]

Status: Recruiting

Cryoneurolysis Versus Radiofrequency in Knee Osteoarthritis

The project will evaluate the effectiveness of Cryoneurolysis versus radiofrequency procedures in adult patients who are resistant to traditional treatment for knee pain. They are a drug-free pain management procedure.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

adults between the ages of 30 and 70 years with a clinical diagnosis of refracto... [+2]

Patients with OA show improvement in pain after physiotherapy. [+6]

Status: Recruiting

Supra-Iliac Anterior Quadratus Lumborum Block and Pericapsular Nerve Group (PENG) Block for Analgesia After Total Hip Arthroplasty

This study aims to compare the analgesic efficacy of supra-iliac anterior quadratus lumborum block (SA-QLB) and pericapsular nerve group (PENG) block in patients undergoing total hip arthroplasty (THA).

Participants needed: 50
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Age from 18 to 75 years. [+3]

Known allergies to the drugs used. [+7]

Status: Recruiting

Ondansetron Lozenge Versus Intravenous for Prevention of Shivering in Cesarean Section

This study aims to compare the effect of ondansetron lozenge and intravenous for prevention of shivering in cesarean section (CS).

Participants needed: 90
Trial details
Age: 18-40Biological sex: FemaleType: InterventionalSponsor: Tanta UniversityUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Age from 18 to 40 years. [+2]

Parturient women with any contraindication or hypersensitivity to the study drug... [+8]

Status: Recruiting

Subtransverse Process Interligamentary Plane Block Versus Rhomboid Intercostal Block Combined With Sub-Serratus Plane Block for Analgesia in Pediatric Thoracotomy

This study aims to compare ultrasound guided subtransverse process interligamentary plane block versus rhomboid intercostal block combined with sub-serratus plane block for postoperative analgesia in pediatric thoracotomy.

Participants needed: 75
Trial details
Age: 6-12Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

Pediatric patients between 6 to 12 years. [+3]

Parents who refused regional anesthesia. [+4]

Status: Not yet recruiting

Fibrinogen-to-Albumin Ratio as a Predictor of Acute Respiratory Distress Syndrome in Traumatic Brain Injury

this study aims to assess the ability of fibrinogen-to-albumin ratio to predict the development of Acute respiratory distress syndrome in traumatic brain injury patients.

Participants needed: 350
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Tanta UniversityUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

Patients ≥ 18 years admitted to the ICU with traumatic Brain Injury [+4]

Preexisting advanced chronic liver disease, nephrotic syndrome, or protein-losin... [+7]

Status: Recruiting

Percutaneous Neurostimulation in Knee Osteoarthritis

Peripheral nerve stimulation (PNS) is a drug-free pain management procedure that uses electrical impulses to target specific nerves and block pain signals. PNS helps decrease perception of pain, providing real answers to patients dealing with chronic knee pain. The case study discussed in this presentation is of the use of PNS targeting the superior lateral genicular nerve and the saphenous nerve for a patient with moderate to severe knee pain from osteoarthritis

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

adults between the ages of 30 and 70 years with a clinical diagnosis of moderate... [+2]

Patients with OA show improvement in pain after physiotherapy. [+6]

Status: Not yet recruiting

Intravenous Lidocaine to Prevent Post-Fundal Pressure Headache During Cesarean Section

This prospective randomized controlled multicenter study will be conducted to evaluate the effects of pre-emptive IV lidocaine dose on the incidence and severity of intraoperative headache that may occur after the extra-abdominal manual uterine fundal pressure in patients undergoing cesarean section under spinal anesthesia.

Participants needed: 680
Trial details
Phase: Phase 3Age: 18+Biological sex: FemaleType: InterventionalSponsor: Tanta UniversityUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Aged ≥ 18 years [+2]

Patients declined to participate in the trial, [+6]

Status: Recruiting

Nicorandil as Anti-inflammatory in Rheumatoid Arthritis

This study aims to evaluate the possible efficacy and safety of nicorandil as anti-inflammatory in managing patients with active rheumatoid arthritis.

Participants needed: 46
Trial details
Phase: Phase 3Age: 18-70Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Patients with active rheumatoid arthritis (not in remission) according to Americ... [+1]

Patients with heart disease (congestive heart failure, arrhythmia and ischemic h... [+5]

Status: Not yet recruiting

Subtransverse Interligamentary Block Versus Paravertebral Block for Quality of Recovery After Mastectomy

This prospective randomized controlled double blinded non-inferiority study will be carried out in Tanta University Hospitals for duration of 6 months from June 2026 to December 2026 on 60 female patients scheduled for unilatral modified radical mastectomy under general anesthesia.

Participants needed: 60
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Tanta UniversityUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Adult female patients aged 18 to 65 years with American Society of Anesthesiolog...

• Patients declined to participate in the trial. [+10]

Status: Not yet recruiting

Subcutaneous Calcitonin in Acute Herpes Zoster

This prospective randomized controlled study will be conducted to evaluate the effect of adding calcitonin to the standard treatment protocol in patients with acute herpes zoster infection.

Participants needed: 168
Trial details
Phase: Phase 3Age: 50+Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

patients aged ≥ 50 years, with acute herpes zoster infection (rash duration < 7...

Coagulation abnormalities [+3]

Status: Not yet recruiting

Oral Versus Intravenous Magnesium on Emergence Delirium

This prospective randomized controlled study will be conducted to compare the effects of preoperative oral magnesium and intraoperative IV magnesium on the incidence and severity of emergence delirium in children undergoing adenotonsillectomy using sevoflurane anesthesia.

Participants needed: 360
Trial details
Phase: Phase 2, Phase 3Age: 4-7Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Children aged 4 to 7 years [+2]

Parents declined to participate in the trial [+5]

Status: Not yet recruiting

ICG in Colon Cancer

The aim of this study is to evaluate the role of indocyanine green (ICG) injection in fluorescence-guided lymphatic mapping during laparoscopic colon cancer resection. This is a single-center prospective single-arm pilot clinical study that will include at least 25 patients with resectable colon cancer. All enrolled patients will undergo intraoperative subserosal ICG-guided lymphatic mapping before dissection, and intravenous ICG perfusion assessment before anastomosis. The primary goal is to determine the proportion of analyzable pN+ patients in whom all metastatic lymph nodes identified on final histopathology are located within the ICG-mapped lymphatic basin.

Participants needed: 25
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 12, 2026
Eligibility criteria

Emergency surgery (obstruction/perforation with sepsis) requiring urgent operati... [+5]

Status: Not yet recruiting

Vitamin D in Diabetic Neuropathy

Introduction Diabetic peripheral neuropathy (DPN) is among the most common chronic complications of diabetes mellitus and represents a major cause of morbidity, impaired quality of life, sleep disturbance, chronic pain, and functional disability.(Kurz et al., 2026) The pathogenesis of DPN is multifactorial and involves oxidative stress, chronic inflammation, endothelial dysfunction, mitochondrial injury, and microvascular ischemia, leading to progressive nerve damage.(Yang et al., 2025) Despite the availability of symptomatic therapies such as gabapentin, pregabalin, and duloxetine, many patients continue to experience persistent neuropathic symptoms, poor sleep quality, and impaired daily functioning. Existing pharmacological therapies are often associated with incomplete response, adverse effects, and high economic burden.(Kaye et al., 2025) Recently, vitamin D has attracted attention beyond its classical role in calcium and bone metabolism. Experimental and clinical evidence suggest that vitamin D possesses neuroprotective, anti-inflammatory, immunomodulatory, and antioxidative properties. Vitamin D receptors are widely distributed in neuronal tissues, Schwann cells, and immune cells, suggesting a potential role in nerve repair and modulation of neuropathic pain pathways.(Liu et al., 2025) Several observational studies have demonstrated a high prevalence of vitamin D deficiency among patients with diabetic neuropathy, and low serum vitamin D levels have been associated with increased neuropathic pain severity and poorer quality of life. However, available interventional studies remain limited and have produced inconsistent findings regarding the therapeutic benefit of vitamin D supplementation in DPN.(Ou et al., 2021) Therefore, this study aims to evaluate whether vitamin D supplementation can improve neuropathic pain, sleep quality, and health-related quality of life among patients with diabetic peripheral neuropathy.

Participants needed: 150
Trial details
Phase: Phase 2, Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 12, 2026
Eligibility criteria

Serum 25(OH)D < 30 ng/mL 6. Stable antidiabetic treatment for at least 3 months

Type 1 diabetes mellitus [+10]

Status: Recruiting

Routine Rehabilitation Versus Shock Wave Therapy for Scapular Dyskinesis

It has been proposed that altered scapular muscle function can contribute to alterations in shoulder kinematics, which often lead to SD and are frequently associated with other shoulder pathologies, such as RC tears, labrum tears, impingement syndrome, and glenohumeral joint instability. However, whether SD leads to the development of these diseases or is a consequence has yet to be clarified. Changes in scapular kinematics can be attributed not only to altered scapular recruitment patterns (e.g., altered serratus anterior muscle activity) or muscle performance (e.g., force imbalance in the upper and lower trapezius muscles) but also to flexibility deficits in the soft tissue surrounding the scapula, which may restrict normal scapular movement during daily activities and sport- specific movements. Although many studies have investigated the optimal management method, to date, there is no consensus. Conservative approaches involve not only physiotherapy but also other techniques, such as extracorporeal shockwave therapy.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

This study included 100 patients with scapular dyskinesis. The patients were div...

History of shoulder or thorax trauma or surgery. [+14]

Status: Recruiting

Dysphagia in Rheumatoid Arthritis

The primary goal of this cross-sectional study is to assess risk factors/predictors for dysphagia severity in RA. The secondary goals include demonstrating whether flexible fiberoptic pharyngolaryngoscopy can diagnose joint-affection-induced dysphagia in patients with rheumatoid arthritis (RA) and whether both oropharyngeal and esophageal dysphagia are present among these patients. The main questions it aims to answer are * What are the predictors that are associated with dysphagia severity via flexible fiberoptic pharyngolaryngoscopy in rheumatoid arthritis patients? * Whether flexible fiberoptic pharyngolaryngoscopy can diagnose joint-affection-induced dysphagia in patients with RA? * Whether both oropharyngeal and esophageal dysphagia are present in patients with RA?

Participants needed: 137
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Tanta UniversityUpdated: Jun 9, 2026Locations: 2
Eligibility criteria

Patients with Rheumatoid arthritis defined by the American College of Rheumatolo... [+1]

concomitant cancer diagnosis, pregnancy. [+6]

Status: Recruiting

A Prospective Comparative Study Evaluating the Safety and Efficacy of Transurethral Thulium Fiber Laser, Holmium Laser and Bipolar Enucleation of Large Sized Prostate

This study compares the safety and efficacy of three endoscopic enucleation techniques for large prostates (\>100 mL) in patients with benign prostatic hyperplasia (BPH): Thulium Fiber Laser Enucleation (ThuFLEP), Holmium Laser Enucleation (HoLEP), and Bipolar Enucleation (B-TUEP). Ninety male patients with severe lower urinary tract symptoms (IPSS ≥20, Qmax ≤10 mL/s) who failed medical therapy will be randomized 1:1:1 into three groups of 30. Primary outcomes include IPSS, quality of life score, maximum flow rate (Qmax), and post-void residual at 1, 3, and 6 months postoperatively. Secondary outcomes include operative time, enucleation efficiency, blood loss, catheterization duration, hospital stay, and complication rates assessed by the Clavien-Dindo classification.

Participants needed: 90
Trial details
Biological sex: MaleType: InterventionalSponsor: Tanta UniversityUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Male patients diagnosed with BPH [+5]

Prostate cancer (current or history). [+8]

Status: Recruiting

US vs FL-Guided Lumbar Nerve Root Injections

The goal of this clinical trial is to learn if ultrasound-guided nerve root injections work as well as fluoroscopy (X-ray)-guided injections to treat lower back and leg pain caused by irritated nerves (lumbosacral radiculopathy) in adults aged 18 to 75 years old. The main questions it aims to answer are: * Does ultrasound guidance lower pain as effectively as fluoroscopy guidance after 3 months? * Does one method help participants recover their ability to do daily activities better than the other? * Are ultrasound-guided injections as fast and safe for participants as fluoroscopy-guided injections? Researchers will compare ultrasound-guided nerve root injections to fluoroscopy-guided nerve root injections to see if ultrasound works to treat the pain just as well while allowing participants to avoid radiation exposure. Participants will: * Receive one targeted nerve injection of medication (a steroid and numbing medicine) in their lower back using either ultrasound or fluoroscopy to guide the needle. * Stay at the clinic for 30 to 60 minutes after the procedure so researchers can check their safety. * Attend checkups at 1 week, 1 month, and 3 months to answer survey questions about their pain levels and daily functioning.

Participants needed: 64
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Adults aged 18 to 75 years. [+4]

Isolated S1 radiculopathy. [+11]

Status: Recruiting

Pelvic Floor Therapies for Lifelong Premature Ejaculation

This randomized controlled trial will compare three pelvic floor-based treatment modalities in men with lifelong premature ejaculation: electromagnetic pelvic floor stimulation, biofeedback-assisted pelvic floor muscle training, and conventional pelvic floor muscle training. A total of 150 men aged 18 to 50 years with lifelong premature ejaculation and stopwatch-measured intravaginal ejaculatory latency time of less than 1 minute will be randomly assigned to one of the three treatment groups. The primary outcome will be the change in intravaginal ejaculatory latency time from baseline to the end of treatment at 6 weeks. Secondary outcomes will include changes in Premature Ejaculation Diagnostic Tool score, International Index of Erectile Function-5 score, patient-reported ejaculatory control, sexual satisfaction, partner satisfaction, treatment adherence, and adverse events.

Participants needed: 150
Trial details
Age: 18-50Biological sex: MaleType: InterventionalSponsor: Tanta UniversityUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Men aged 18 to 50 years. [+4]

Erectile dysfunction. [+2]

Status: Recruiting

Combination of Superior Hypogastric Plexus Block and Transversus Abdominis Plane Block in Abdominal Hysterectomies

This study aims to evaluate the analgesic effect of superior hypogastric plexus block combined with transversus abdominis plane block in abdominal hysterectomies.

Participants needed: 44
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Tanta UniversityUpdated: May 27, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years. [+2]

History of allergies to local anesthetics. [+7]

Status: Not yet recruiting

Measuring the Changes of the Intraocular Pressure After Corneal Cross Linking Using Corvis CT

To evaluate the changes that occur in the intraocular pressure before and after corneal cross linking using Corvis CT.

Participants needed: 1
Trial details
Age: 19-35Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: May 20, 2026
Eligibility criteria

Patients who will corneal cross linking for mild degree of keratoconus, age betw...

Corneal scarring. [+4]