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Recruiting NCT07183501

Combined Hystroscopic and Laparoscopic Repair of CS Scar Disorder

No phase Interventional Cesarean Section Complications Abnormal Uterine Bleeding

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Combined hystroscopic and laparoscopic repair.
Who it may be relevant to
Registry conditions: Cesarean Section Complications, Abnormal Uterine Bleeding. Basic parameters: 20 years — 45 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

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

Interventions

  • Procedure Combined hystroscopic and laparoscopic repair
    Hystroscopic isthmoplasty will be done first to ensure removal of chronically inflamed Unhealthy edges of niche, then laparoscopic exison of scar will be dine, followed by repair of the defect

Primary outcome measures

  • change in Residual Myometrial Thickness [Time frame: 3 months]
Secondary outcome measures (1)
  • Number of patients complete resolution of symptoms [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • symptomatic uterine Niche :postmenstrual spotting

Exclusion criteria

  • contraindications for endoscopy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Assiut university, women health hospital — Asyut

Identifiers

NCT: NCT07183501 · Managment of CS scar disorder

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗