Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
ID06466343

Immunohistopathologic Findings and Surgical Repair of Cesarean Scar Niche Using Hysteroscopy Study of Tissue Changes and Symptom Improvement in Women with Cesarean Scar Defects

Led by Sohag University · Updated on 2024-06-20

50

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying women with symptomatic uterine scar niches, which are pouch-like defects on the anterior wall of the uterine isthmus where a previous cesarean section (CS) scar was made. These niches are defined as depressions in the myometrium of at least 2 mm. The study aims to identify the histopathologic characteristics of cesarean scar niche specimens removed by hysteroscopy and to help gynecologists understand the effectiveness of hysteroscopic repair for improving symptoms and fertility. The surgical treatment involves operative hysteroscopy performed postmenstrual. Patients receive cervical preparation with misoprostol before surgery. During the procedure, a resectoscope is used to trim the lower edge of the niche and coagulate the base. The removed tissue is collected for detailed histopathological and immunohistochemical examination, including analysis of inflammation, fibrosis, and immune markers. Follow-up occurs three months after surgery. Participants are assessed with transvaginal ultrasound to measure niche dimensions and residual myometrial thickness. Clinical data such as age, parity, previous surgeries, and symptoms are collected. After three months, symptom improvement and quality of life are evaluated through ultrasound and questionnaires. Researchers measure pathological variations in niche specimens to better understand causes of uterine scar thinning and monitor patient outcomes.

CONDITIONS

Official Title

Immunohistopathologic Findings of Cesarean Scar Niche

Who Can Participate

Age: 18Years - 45Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women with a history of one or more cesarean sections performed more than one year ago
  • Diagnosed with cesarean scar defect by transvaginal ultrasound
Not Eligible

You will not qualify if you...

  • Women diagnosed with pelvic inflammatory disease
  • Women suspected of having gynecological malignancy
  • Postmenopausal women
  • Women with heart disease
  • Women with liver disease
  • Women with kidney impairment
  • Women with bleeding tendency

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sohag University Hospitals

Sohag, Egypt

Actively Recruiting

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Research Team

M

mohamed Ab Galal, A.Lecturer

A

Amr O Abelkareem, A.lecturer

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

Frequently Asked Questions

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