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Comparison of Operated Ruptured and Non-ruptured Endometriomas

Comparison of Inflammatory Parameters in Operated Ruptured and Non-ruptured Endometriomas

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05348070
Acronym
RupturedOMA
Enrollment
181
Registered
2022-04-27
Start date
2014-01-01
Completion date
2021-06-20
Last updated
2022-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometrioma, Endometriosis Ovary, Ruptured Endometrioma

Keywords

endometrioma, rupture, endometriosis

Brief summary

Ruptured endometrioma cases were compared with unruptured endometrioma cases.

Detailed description

This study aims to compare the findings in patients who had surgery for ruptured endometrioma with the patients who had an unruptured endometrioma. This study was conducted at Republic of Turkey Ministry of Health, Health Science University Etlik Zübeyde Hanım Gynecology Training and Research Hospital Infertility Clinic and all patients who were operated for endometrioma and had a histopathology report confirming the presence of endometrioma between January 2014 and December 2020 were included. In this study, demographic characteristics, intraoperative findings, laboratory values and follow-up recommendations of two groups compared. The patients' age, presence of sexual activity and/or infertility, gravidity, parity, abortion, history of ectopic pregnancy, accompanying systemic disease, previous operations, drug use, and symptoms were recorded. Preoperative and postoperative complete blood count, Cancer antigen 125 (CA 125), Cancer antigen 19-9 (CA19-9), Cancer antigen 15-3 (CA 15-3), Carcinoembryonic antigen (CEA), alpha fetoprotein (AFP), anti mullerian hormone (AMH), fibrinogen, C-reactive protein (CRP) values of the patients were obtained. Patient files, operation notes and laboratory values of the electronic recording system database and the two groups were compared.

Interventions

All patients included in the study were operated patients.

Sponsors

EZH EAH
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
16 Years to 48 Years
Healthy volunteers
No

Inclusion criteria

* All patients who were operated on in Republic of Turkey Ministry of Health, Health Science University Etlik Zübeyde Hanım Gynecology Training and Research Hospital Infertility Clinic, whose histopathological diagnosis was confirmed as endometrioma, and who did not meet the

Exclusion criteria

, were included in the study.

Design outcomes

Primary

MeasureTime frameDescription
Pre-interventional Comparison of inflammatory parametersBlood samples were taken from the patients before the surgeryNeutrophil/Lymphocyte ratio (NLR), Platelet/Lymphocyte ratio (PLR), Monocyte/Lymphocyte ratio (MLR) were compared between two groups in the preoperative period
Comparison of inflammatory parameters after surgeryBlood samples were taken from the patients in the first postoperative day.Neutrophil/Lymphocyte ratio (NLR), Platelet/Lymphocyte ratio (PLR), Monocyte/Lymphocyte ratio (MLR) were compared between two groups in the postoperative period
Pre-interventional Comparison of tumor markersBlood samples were taken from the patients before the surgeryCancer antigens; CA125, CA19-9 and CA 15-3 were compared between two groups in the preoperative period
Comparison of tumor markers after surgeryBlood samples were taken from the patients after the surgery up to 24 weeksCancer antigens; CA125, CA19-9 and CA 15-3 were compared between two groups in the postoperative period

Secondary

MeasureTime frameDescription
Sexual activityBefore surgeryThe existence of sexual activity in each study group was questioned.
InfertilityBefore surgeryThe existence of infertility in each study group was questioned.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026