Actively Recruiting
Combined Hystroscopic and Laparoscopic Repair of Cesarean Section Scar Disorder
Led by Assiut University · Updated on 2025-09-19
30
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research evaluates a new combined hystroscopic and laparoscopic technique to repair symptomatic uterine niches, which are complications related to cesarean section scars. The study aims to improve symptom resolution and increase residual myometrial thickness after repair. Women experiencing postmenstrual spotting due to uterine niche are the focus of this study. Participants will undergo a two-step procedure starting with hystroscopic isthmoplasty to remove unhealthy scar tissue edges, followed by laparoscopic excision of the scar and repair of the uterine defect. This combined approach is being studied to maximize symptom relief and tissue restoration. During the study, researchers will monitor changes in residual myometrial thickness three months after the procedure and assess the number of patients who experience complete symptom resolution at the same timepoint. The total participation duration includes follow-ups to evaluate these primary and secondary outcomes under medical supervision.
CONDITIONS
Brief Title
Combined Hystroscopic and Laparoscopic Repair of CS Scar Disorder
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Symptomatic uterine niche with postmenstrual spotting
You will not qualify if you...
- Contraindications for endoscopy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 1 week
Participants undergo combined hystroscopic and laparoscopic repair of the cesarean section scar, followed by immediate post-operative care.
1 surgical visit and several post-operative visits
Duration - 3 months
Participants are monitored for recovery and resolution of symptoms after surgery.
Approximately 3 follow-up visits
Trial Site Locations
Total: 1 location
1
Assiut university, women health hospital
Asyut, Asyut Governorate, Egypt, 71511
Actively Recruiting
Research Team
A
Abdulrahman Rageh, Lecturer
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here