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OpenTrials
Completed

NCT Number: NCT06421857

Hemostatic Measures During Laparoscopic Cystectomy for Endometrioma

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

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Ain Shams university

Cairo, 11566, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Suturing

Procedure

laparoscopic cystectomy for endometrioma and hemostasis was done using suturing

bipolar electrocoagulation

Procedure

laparoscopic cystectomy for endometrioma and hemostasis was done bipolar electrocoagulation

Primary outcomes

  1. ovarian reserve

    Time frame: 6 weeks after procedure

    measuring AMH level

Sponsors and collaborators

Lead sponsor

Ain Shams Maternity Hospital

Other

Registry information

Official study title

Bipolar Coagulation Versus Suturing During Laparoscopic Endometriotic Cystectomy

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
May 20, 2024
Registry last updated
May 20, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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