Clinical Trials Logo

Filter by:
NCT ID: NCT06276777 Not yet recruiting - Clinical trials for Dentin Hypersensitivity

The Effect of Using Desensitizers Containing S-PRG In Treatment Of Dentin Hypersensitivity Over 6 Months: A Randomized Clinical Trial

S-PRG
Start date: May 1, 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare the effect of desensitizer containing S-PRG have similar effect as sodium fluoride with functionalized tri-calcium phosphate containing desensitizer in relieving dentinal hypersensitivity in adult patients for six months follow-up. patients will be asked to report pain degree on the visual analogue scale (VAS) along the follow up periods on both groups.

NCT ID: NCT06267885 Not yet recruiting - Clinical trials for Fracture Neck of Femur

Fixation of Fracture Neck of Femur in Children

Start date: March 2024
Phase: N/A
Study type: Interventional

Find the best way for fixation of fracture neck of femur in children either by cannulated screws or wagner's technique

NCT ID: NCT06267066 Not yet recruiting - Clinical trials for Lichen Simplex Chronicus

Fractional Carbon Dioxide Laser: A Novel Therapeutic Option for Lichen Simplex Chronicus

Start date: March 1, 2024
Phase: N/A
Study type: Interventional

The goal of this randomized control trial is to compare the use of fractional carbon dioxide (Co2) laser to topical corticosteroids to treat lichen simplex chronicus (LSC) patients presenting to Dermatology outpatient clinic, Faculty of Medicine, Cairo University. Participants will: - Be assessed clinically by doctor - Biopsies will be taken from them by doctor - Receive treatment as laser or topical steroids or both - Fill in depression questionnaire. Researchers will divide and compare groups as follows: Sixty patients will be divided randomly through closed envelop technique into 2 groups (Group A and B) each of 30 patients. Group A will be subdivided into 2 groups (1 and 2). All LSC lesions will be treated in any patient having multiple lesions. - Group 1 - A: Patients will receive 3 monthly laser sessions, in addition to the use of topical emollients only once daily in between the sessions. - Group 2 - A: Patients will receive 3 monthly laser sessions, in addition to topical steroids twice daily and topical emollient once daily in between the sessions. - Group B: Patients will be prescribed topical steroids twice daily and topical emollient once daily for 3 months. to see if: 1. Pruritus severity scale. 2. Scaling, erythema, lichenification excoriation scores 3. Visual analogue scale. 4. Investigator's Global Assessment. 5. Itching mediators (Interleukin-31, Nerve Growth Factor and Substance P assays (itching mediators) 6. Depression improve more in which group of patients after treatment.

NCT ID: NCT06265896 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Effect of Kinesiotaping on Activation of Abdominal Muscles in Female Patients With Stress Urinary Incontinence

Start date: March 1, 2024
Phase: N/A
Study type: Interventional

This study will be conducted to evaluate the effect of kinesiotaping on activation of abdominopelvic cavity for management of stress urinary incontinence females' patients.

NCT ID: NCT06265454 Not yet recruiting - Myopia Progression Clinical Trials

Low Dose Atropine Eye Drops in Myopic Egyptian Children

LAMP
Start date: September 1, 2024
Phase: Phase 2
Study type: Interventional

Previous Studies reported that low concentration atropine eye drops may be effective in increasing the choroidal blood flow and thickness and this slows myopia progression. purpose of the study is to compare changes in axial length, anterior chamber depth, choroidal thickness, central corneal thickness and anterior scleral thickness among myopic children receiving atropine 0.05% or 0.01% and placebo.

NCT ID: NCT06265324 Not yet recruiting - Drug-coated Balloon Clinical Trials

Drug-coated Balloon Treatment in Coronary Lesions

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

This study is multicenter registry for drug-coated balloon treatment for de novo and in-stent restenosis lesions

NCT ID: NCT06264401 Not yet recruiting - Clinical trials for Postmenopausal Osteoporosis

Treatment Exercises With Core Stability and Dynamic Resistance Exercise for Postmenopausal Women With Osteoporosis

Start date: February 22, 2024
Phase: N/A
Study type: Interventional

osteoporosis is a common disease that affect most of postmenopausal women. various treatment procedures are used to avoid future complain among postmenopausal population.

NCT ID: NCT06262893 Not yet recruiting - Dexamethasone Clinical Trials

Effect of Dexamethasone Adjuvant in Combined Supraclavicular Block and Suprascapular Block Versus Interscalene Block in Patients Undergoing Shoulder Arthroscopy

Start date: February 25, 2024
Phase: N/A
Study type: Interventional

In this study the investigators aim to compare the effect of the suprascapular- supraclavicular nerve block in association with dexamethasone to that of the interscalene brachial plexus block on analgesic effect during arthroscopic shoulder surgery, as postoperative pain scores ,postoperative consumption of analgesic rescue medications and diaphragmatic excursion assessment.

NCT ID: NCT06262490 Not yet recruiting - Clinical trials for Pelvic Floor Disorders

Impact of Pelvic Floor Rehabilitation Combined With Ultrasound Therapy on Osteomyoarticular Symptoms in Chronic Perineal Pain

Start date: March 1, 2024
Phase: N/A
Study type: Interventional

The purpose of the study is to find out the effect of pelvic floor rehab combined with ultrasound have effect in chronic perineal pain subjects associated with osteomyoarticular symptoms .

NCT ID: NCT06255314 Not yet recruiting - Ventral Hernia Clinical Trials

Minimally Invasive Techniques in Ventral Hernioplasty

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

1. Review the surgical outcome of different techniques using extraperitoneal ventral hernia repair regarding postoperative pain. wound infection ,hospital stay , recurrence ,mesh migration and mesh induced visceral complications. 2. Reviewing advantages and drawbacks of each surgical technique regarding feasibility ,cost effectiveness and technical difficulties