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Clinical Trials/NCT07183501
NCT07183501RecruitingNot Applicable

Combined Hystroscopic and Laparoscopic Repair of CS Scar Disorder

Assiut University1 site in 1 country30 target enrollmentStarted: June 1, 2024Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
30
Locations
1
Primary Endpoint
change in Residual Myometrial Thickness
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Combined hystroscopic and laparoscopic repair of symptomatic uterine Niche as new technique to maximize resolution of symptoms after niche repair with concomitant increase in RMT

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •symptomatic uterine Niche :postmenstrual spotting

Exclusion Criteria

  • •contraindications for endoscopy

Arms & Interventions

Patients with symptomatic uterine niche

Experimental

Intervention: Combined hystroscopic and laparoscopic repair (Procedure)

Outcomes

Primary Outcomes

change in Residual Myometrial Thickness

Time Frame: 3 months

in mm

Secondary Outcomes

  • Number of patients complete resolution of symptoms(3 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Abdulrahman Muhammad Rageh

Lecturer

Assiut University

Study Sites (1)

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