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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06132009
Other study ID # 2023/05/11/030
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 22, 2022
Est. completion date February 1, 2024

Study information

Verified date November 2023
Source Bagcilar Training and Research Hospital
Contact Evrim Ebru Kovalak, MD
Phone 905324628989
Email evrimebru@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To investigate the effect of preoperative evaluation parameters in predicting recurrent disease in women who have undergone cystectomy or unilateral salpingo-oophorectomy due to endometriosis.


Description:

Endometriosis is an estrogen-dependent gynecological disease characterized by the presence of endometrial-like tissue outside the uterine cavity, associated with pelvic pain and subfertility. Despite its benign character, endometriosis can recur after surgery and continues to be a disease that disrupts the quality of life of millions of women. This study aimed to examine the risk factors in women who underwent cystectomy or unilateral salpingo-oophorectomy due to endometriosis but had a recurrence. Therefore, the predictive value of parameters such as preoperative biochemical parameters, cyst size and the revised American Society for Reproductive Medicine (rASRM) Scoring system will be examined in recurrent cases.


Recruitment information / eligibility

Status Recruiting
Enrollment 64
Est. completion date February 1, 2024
Est. primary completion date January 1, 2024
Accepts healthy volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Surgery of endometriosis
Cystectomy or unilateral oophorectomy due to endometriosis

Locations

Country Name City State
Turkey Bagcilar Teaching and Research Hospital Istanbul Bagcilar

Sponsors (1)

Lead Sponsor Collaborator
Bagcilar Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Hidari T, Hirata T, Arakawa T, Koga K, Neriishi K, Fukuda S, Nakazawa A, Nagashima N, Ma S, Sun H, Takamura M, Harada M, Hirota Y, Wada-Hiraike O, Fujii T, Osuga Y. Contralateral ovarian endometrioma recurrence after unilateral salpingo-oophorectomy. BMC — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Prediction of endometriosis recurrence Which women are more likely to have recurrence after endometriosis surgery? 6-180 months
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