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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04639063
Other study ID # PMS20-11-01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 17, 2020
Est. completion date December 20, 2020

Study information

Verified date March 2021
Source Al-Azhar University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A retrospective review of all patients who underwent surgery for an anterior abdominal wall mass which confirmed by pathology examination as an endometrioma will be completely performed. The clinical data will be recorded and pathology report diagnosis will be correlated with the clinical data to assess the possible causes of endometrioma in the women treated in our tertiary hospital and the efficacy of the surgical excision.


Description:

Our hospital is a tertiary center for performing Cesarean sections, external endometriosis (Endometrioma) is a challenging complication for this operation, many treatment choices are available and the most common is the surgical excision, however recurrence could be seen after the surgical operation. We assess all patients who underwent surgical excision for abdominal wall endometriomas in our hospital by retrieving the medical files and pathology reports to study the possible age group,causes and duration of endometriomas. Also the rate of enodmetriomas among the previously experienced females with cesarean section operations. Pathological diagnosis tools will be also assessed. Ethical approval was obtained from the local committee. Results will be statistically assessed using SPSS programm.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 20, 2020
Est. primary completion date December 15, 2020
Accepts healthy volunteers No
Gender Female
Age group 15 Years to 65 Years
Eligibility Inclusion Criteria: - Female - Surgically removed abdominal wall endometrioma Exclusion Criteria: - Male (very very rare to occur) - medically treated enodmetrioma - Outside treated patients

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Microscopic examination using H&E stained slides
Reexamination of the stained slides of the patients from the hospital archive and adding a CD10 stain when required

Locations

Country Name City State
Egypt Abdulkarim Hasan Cairo

Sponsors (1)

Lead Sponsor Collaborator
Al-Azhar University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Positive for endometrioma Presence of endometrial glands and stroma along with hemosidren pigment under microscopic examination, confirms the diagnosis and the case will be calculated and the related clinical data 1 day
See also
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Completed NCT03332004 - Near-infrared Fluorescence Imaging as a Supportive Tool for Localisation of Deep Infiltrating Endometriosis During Laparoscopy Phase 2