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Clinical Trials/CTRI/2025/12/098752
CTRI/2025/12/098752
Not yet recruiting
Not Applicable

Pre operative assessment to predict associated endometriosis in women with fibroids undergoing surgery

Diksha Goyal1 site in 1 country52 target enrollmentStarted: December 20, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Diksha Goyal
Enrollment
52
Locations
1
Primary Endpoint
To find correlation between clinical and USG findings with per op presence of endometriosis

Overview

Brief Summary

The coexistence of endometriosis and uterine fibroids presents significant diagnostic and therapeutic challenges. Advancements in imaging techniques, scoring systems, and predictive modeling offer promising avenues for enhancing preoperative assessment. A comprehensive approach that integrates clinical evaluation, advanced imaging, and intraoperative findings is crucial for the effective management of women with these concurrent gynecological conditions

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • women aged 18 or older, previously or newly diagnosed with uterine fibroids, undergoing myomectomy or hysterectomy.

Exclusion Criteria

  • women less than 18 years of age women who are post menopausal women who have history of more than one course of PID treatment.

Outcomes

Primary Outcomes

To find correlation between clinical and USG findings with per op presence of endometriosis

Time Frame: baseline, 2 year

To evaluate the correlation between intra operative assessment of endometriotic adhesion scores (r-ASRM score) and relevant clinical or diagnostic parameters

Time Frame: baseline, 2 year

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Diksha Goyal
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

DIKSHA GOYAL

Kasturba Medical college, MAHE, Manipal

Study Sites (1)

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