Actively Recruiting
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
Eligibility Criteria
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
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
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Trial Site Locations
Total: 1 location
1
Sohag University Hospitals
Sohag, Egypt
Actively Recruiting
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
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