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NCT ID: NCT06253442 Recruiting - Clinical trials for Proximal Humerus Fractures

Comparison Between Interscalene Block and Combined Suprascapular and Axillary Blocks for Proximal Humerus Fracture Surgeries.

Start date: February 10, 2024
Phase: N/A
Study type: Interventional

A Comparative study Between Ultrasound guided Interscalene Block and Combined Ultrasound guided suprascapular and axillary nerve blocks for proximal humerus fracture Surgeries. The aim of this study is to investigate whether (Suprascapular nerve block) and (Axillary nerve block) are effective in providing analgesia for shoulder surgery as an (Interscalene block), while minimizing the occurrence of hemi-diaphragmatic paralysis. We hypothesized that analgesia with a (Suprascapular nerve block and Axillary nerve block) would be noninferior compared with patients receiving an interscalene block and the incidence of hemi-diaphragmatic paralysis would be significantly lower with (Suprascapular nerve block and Axillary nerve block) in proximal humerus fracture surgeries.

NCT ID: NCT06253429 Recruiting - Type 1 Diabetes Clinical Trials

Alpha-lipoic Acid in Diabetic Nephropathy

Start date: January 1, 2023
Phase: Phase 3
Study type: Interventional

Endothelial dysfunction in diabetes is a central event in the pathogenesis of different microangioapthic changes. Nephropathy in patients with type 1 diabetes is a severe microvascular complication.

NCT ID: NCT06252441 Recruiting - Clinical trials for Post ERCP Pancreatitis

Comparative Clinical Study to Evaluate the Possible Efficacy and Safety of Oral N-Acetyl Cysteine Versus Rectal Diclofenac in the Prevention of Post Endoscopic Retrograde Cholangiopancreatography Pancreatitis

Start date: February 2024
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of the current study is to compare the efficacy and safety of oral NAC and rectal diclofenac in preventing Post Endoscopic retrograde cholangiopancreatography Pancreatitis. .

NCT ID: NCT06252181 Recruiting - Clinical trials for Peripheral Arterial Disease

Pain and Hemodynamics in Peripheral Arterial Disease: Response to Pulsed Electromagnetic Treatment

Start date: December 15, 2022
Phase: N/A
Study type: Interventional

patients with peripheral arterial disease are recommended to perform all exercise forms including elliptical type. electromagnetic treatment addition to exercise may increase benefits of this exercise

NCT ID: NCT06251661 Recruiting - Stroke Clinical Trials

Cognitive Multi-sensory Rehabilitation on Upper Limb Function and Fatigue in Stroke

Start date: February 1, 2023
Phase: N/A
Study type: Interventional

This interventional study aims to investigate the therapeutic efficacy of Cognitive multi-sensory rehabilitation (CMR) on upper limb function and fatigue in chronic stroke patients. The main question is: • Does cognitive multi-sensory rehabilitation significantly affect upper limb function and fatigue in stroke patients? Participants will be assigned into two groups. They will receive 12 sessions of study group CMR and traditional physical therapy and control group traditional physical Therapy rehabilitation. CMR 40 minutes immediately followed by 20 minutes of selected physical therapy program, three sessions per week for four weeks.

NCT ID: NCT06249607 Recruiting - Insomnia Clinical Trials

Impact Of Mindfulness Breathing Versus Storytelling On Non- Specific Insomnia In Elderly

Start date: January 5, 2024
Phase: N/A
Study type: Interventional

This study will be conducted to compare between effects of mindfulness breathing and storytelling on insomnia in the elderly.

NCT ID: NCT06249503 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Ultrasound Guided Activated and Non Activated Platelet Rich Plasma Injection Versus Hydro Dissection by Steroids.

PRP
Start date: February 1, 2023
Phase: Phase 4
Study type: Interventional

PRP represents a promising, nonsurgical option for patients with carpal tunnel syndrome (CTS) with improvement in symptoms compared to placebo, conservative treatment, and local corticosteroid injections at 3-months postintervention. However, the lack of significant long-term results in pain and function demands the presence of future studies to further determine the long-term effect on a large group of homogeneous patients. More over to determine the clinical indications, effect on differing CTS severities, and the effects of preparation, concentration of the platelets and methods of activation of PRP

NCT ID: NCT06249100 Recruiting - Renal Stone Clinical Trials

Flexible Mini Percutaneous Nephrolithotomy vs Retrograde Intra-renal Surgery

Start date: January 1, 2024
Phase: Phase 2/Phase 3
Study type: Interventional

The use of flexible ureteroscopy and minimally-invasive percutaneous techniques, which utilize smaller tract sizes, has been established as a way to decrease the invasiveness of procedures and improve patient outcomes compared to conventional percutaneous nephrolithotomy (PCNL) and flexible mini-PCNL has emerged as a novel technique previously first as an auxiliary procedure and then as a standalone technique. This study aims to assess the feasibility and effectiveness of flexible nephoscopy in improving stone clearance compared to standard retrograde intrarenal surgery using a flexible ureteroscope.

NCT ID: NCT06248931 Recruiting - Migraine Disorders Clinical Trials

Valproate Versus Topiramate in Migraine

Start date: February 1, 2024
Phase: Phase 3
Study type: Interventional

Investigators aim to compare the effect of valproate versus topiramate in migraine by assessing the absolute reduction in MMD in each group, the percentage of patients who achieved ≥ 50% reduction in the monthly headache days frequency compared to the baseline frequency.

NCT ID: NCT06246682 Recruiting - Clinical trials for Cholesteatoma, Middle Ear

Impact of Mastoid Condition on Results of Endoscopic Management of Cholesteatoma

Start date: February 10, 2024
Phase: N/A
Study type: Interventional

The goal of this interventional study is to learn about the effect of mastoid process status and the method of ossicular reconstruction on the results of the procedure transcanal endoscopic management of patients with localized atticoantral cholesteatoma