Evaluating preoperative factors to predict endometriosis recurrence
Predictive Value of Preoperative Evaluation in Cases of Recurrent Endometriosis
This study is trying to see if certain factors before surgery can help predict if endometriosis will come back in women who have had surgery to remove cysts or ovaries.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 64 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | Female |
| Sponsor | Bagcilar Training and Research Hospital Government |
| Locations | 1 site (Istanbul, Bagcilar) |
| Trial ID | NCT06132009 on ClinicalTrials.gov |
What this trial studies
This observational study investigates how preoperative evaluation parameters can predict the recurrence of endometriosis in women who have undergone cystectomy or unilateral salpingo-oophorectomy. It focuses on identifying risk factors such as preoperative biochemical markers, cyst size, and the revised American Society for Reproductive Medicine (rASRM) scoring system. By analyzing these parameters, the study aims to improve understanding of recurrence patterns and enhance patient outcomes following surgery for endometriosis.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18-50 who have undergone cystectomy or unilateral oophorectomy due to endometriosis.
Not a fit: Patients who have had bilateral oophorectomy due to endometriosis, those with malignant conditions, smokers, or individuals with autoimmune diseases may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to better preoperative assessments and tailored surgical approaches, potentially reducing the recurrence of endometriosis.
How similar studies have performed: While the predictive evaluation of preoperative factors in endometriosis is a relevant area of research, this specific approach appears to be novel and untested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women aged 18-50 who had a cystectomy or unilateral oophorectomy due to endometriosis Exclusion Criteria: * Women who have had bilateral oophorectomy due to endometriosis * Malignant conditions * Smoking * Women with autoimmune disease
Where this trial is running
Istanbul, Bagcilar
- Bagcilar Teaching and Research Hospital — Istanbul, Bagcilar, Turkey (Recruiting)
Study contacts
- Principal investigator: Evrim Ebru Kovalak, MD — Bagcilar Training and Research Hospital
- Study coordinator: Evrim Ebru Kovalak, MD
- Email: evrimebru@yahoo.com
- Phone: 905324628989
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.