Viewing Study NCT06796933


Ignite Creation Date: 2025-12-25 @ 3:00 AM
Ignite Modification Date: 2026-01-01 @ 3:58 AM
Study NCT ID: NCT06796933
Status: NOT_YET_RECRUITING
Last Update Posted: 2025-01-28
First Post: 2025-01-22
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Effect of Bioptron on Scar Formation After Cesarean Section
Sponsor: Cairo University
Organization:

Study Overview

Official Title: Effect of Bioptron on Scar Formation After Cesarean Section: a Randomized Controlled Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2025-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of the study will be to determine the effect of polarized light therapy (Bioptron) on scar formation after a cesarean section.
Detailed Description: Cesarean deliveries are among the most frequently performed surgical procedures for women worldwide, with their prevalence increasing globally, especially in developing nations like Egypt.

A scar is a natural outcome of the healing process following a wound. Complaints associated with scars can lead to both physical discomfort and psychological challenges. Enhanced healing of CS scars could lead to better postoperative outcomes, reducing complications such as infection, pain, and restricted mobility. These aspects of recovery are often neglected, as noted by.

This study will be the first to specifically examine the effects of Bioptron light therapy on CS scar formation. While previous research has shown the benefits of this therapy on scars from various operations, none have focused on CS scars. By investigating this innovative, non-invasive treatment approach, the study aims to fill a critical gap in existing research and offer valuable insights into managing and improving postoperative recovery for CS patients.

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: