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Incision clinical trials

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NCT ID: NCT06114823 Completed - Clinical trials for Carpal Tunnel Syndrome

Comparing a Modified Mini-incision Approach Versus the Conventional Approach for Carpal Tunnel Release

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

Carpal tunnel syndrome (CTS) is the commonest nerve compression syndrome in the upper limbs, and carpal tunnel decompression is one of the most prevalent upper limb surgical interventions. Surgeries for CTS may be more effective compared to conservative measures in reducing symptoms and improving hand function, particularly in patients with severe CTS. The etiology of CTS is multifactorial and includes occupational and personal factors. Physical workload factors play an important role in CTS but the role of some personal factors is less clear. Obesity is a well-documented risk factor for CTS. Hypothyroidism, diabetes mellitus, rheumatoid arthritis and osteoarthritis are possible risk factors for CTS. Finally, the role of smoking in CTS is uncertain. Traditional approach makes use of a longitudinal skin incision from the palm toward the wrist and across the transverse carpal ligament. Though this approach offers excellent visualization, reliable release of the full retinaculum, and ability to identify anatomic variations, it is associated with some intractable complications, including wound pain, scar tenderness, flexor tendon entrapment and thenar as well as hypothenar (pillar) pain, which are difficult to recovery. The attempt to perform CTR without extra complications leads to the development of different techniques and several mini-incision approaches. These techniques help to reduce incisional discomfort after surgery, but it can lead to frequent incidence of blood vessel injury or incomplete release. The mini-incision approaches have the advantage of leaving a smaller scar, less scar pain, and lower grade of pillar pain. Though several methods have been proposed, there were still some disadvantages in them. Though CTR can be safely accomplished by them, incomplete release still occurred in several cases for some reasons. After intensive research in the current literature, there is a paucity of studies evaluating the efficacy and safety of mini-incision approaches in achieving CTR in Egyptian patients. That is why we conducted the present study to present our experience with the modified mini-incision technique and compare its outcomes to the conventional open approach.

NCT ID: NCT05963477 Completed - Wound Dehiscence Clinical Trials

Pediatric Post-operative Abdominal Wound Dehiscence in Association With Midline vs Other Incisions: A Prospective Cohort Study

Start date: November 1, 2018
Phase:
Study type: Observational

This study is designed to see different abdominal incisions complication among neonates, infants and children and to find risk factors for developing wound dehiscence

NCT ID: NCT05240248 Completed - Laceration Clinical Trials

Optilene® Suture Material for Dermal Sutures

OPTIDERMAL
Start date: June 22, 2022
Phase:
Study type: Observational

In this non-interventional study, Optilene® suture will be evaluated for skin closure in adult patients.

NCT ID: NCT04464304 Completed - Surgery Clinical Trials

Virtual Reality for Postoperative Pain Management

Start date: July 11, 2020
Phase: N/A
Study type: Interventional

This trial studies an active virtual reality (VR) experience as a means for non-pharmacologic postoperative pain management among patients after head and neck surgery. Investigators will assess differences in pain scores, analgesic use, and subjective patient experiences between patients participating in a VR activity and patients participating in the same activity using a smartphone.

NCT ID: NCT03026400 Completed - Clinical trials for Patient Satisfaction

Sub vs Trans-umbilical Incision: A Patient's Satisfaction-centered Trial

Start date: August 2014
Phase: N/A
Study type: Interventional

While some studies have suggested that subumbilical and transumbilical incisions have a similar clinical efficiency and safety, no study has yet evaluated their respective impact on patient's postoperative aesthetic satisfaction. The objective of this randomised trial is to compare patient's postoperative aesthetic satisfaction depending on the type of incision which is performed during surgeries.