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NCT06421857 Clinical Trial

Hemostatic Measures During Laparoscopic Cystectomy for Endometrioma

Endometrioma Clinical Trial

Official title:
Bipolar Coagulation Versus Suturing During Laparoscopic Endometriotic Cystectomy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06421857
Other study ID # ASU Hemostasis
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2023
Est. completion date May 1, 2024

Study information
Verified date May 2024
Source Ain Shams Maternity Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

laparoscopic excision of ovarian endometriotic cysts is generally recommended because it has been associated with a higher spontaneous conception rate, residual ovarian function after the procedure may be affected

Recruitment information / eligibility
Status Completed
Enrollment 48
Est. completion date May 1, 2024
Est. primary completion date May 1, 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - 18 to 35 years - unilateral endometriotic cyst Exclusion Criteria: anovulatory women women with decreased ovarian reserve women receiving hormonal treatment three months prior to surgery women with any contraindication to laparoscopy women with previous ovarian surgery possible ovarian malignancy.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• suturing
laparoscopic cystectomy for endometrioma and hemostasis was done using suturing
• bipolar electrocoagulation
laparoscopic cystectomy for endometrioma and hemostasis was done bipolar electrocoagulation

Locations
Country Name City State
Egypt Ain Shams university Cairo

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams Maternity Hospital

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary ovarian reserve measuring AMH level 6 weeks after procedure
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