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Clinical Trials/NCT06047730
NCT06047730
Completed
Not Applicable

Clinical Effect Evaluation of Laparoscopic Surgery for Ovarian Benign Tumors by Different Approaches

Yingchun Ma1 site in 1 country173 target enrollmentJanuary 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Laparoscope
Sponsor
Yingchun Ma
Enrollment
173
Locations
1
Primary Endpoint
peroperative bleeding
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Main purpose: To compare the intraoperative and postoperative recovery of laparoscopic surgery for ovarian benign tumors through different approaches; Secondary objective: Will vNOTES increase the risk of cesarean section during pregnancy and affect the quality of sexual life after surgery.

Registry
clinicaltrials.gov
Start Date
January 1, 2017
End Date
March 31, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Yingchun Ma
Responsible Party
Sponsor Investigator
Principal Investigator

Yingchun Ma

Clinical Effect Evaluation of Laparoscopic Surgery for Ovarian Benign Tumors by Different Approaches

Qianfoshan Hospital

Eligibility Criteria

Inclusion Criteria

  • Preoperative consideration was for benign ovarian tumors requiring surgical treatment.

Exclusion Criteria

  • (1) Ovarian malignant tumor or borderline tumor was considered before surgery or proved during surgery. (2) Severe endometriosis, previous severe pelvic inflammation, peritonitis, and other serious pelvic adhesions are considered. (3) Pregnancy status. (4) Postoperative follow-up is not convenient and lost visitors.

Outcomes

Primary Outcomes

peroperative bleeding

Time Frame: during the operation time

peroperative bleeding

Secondary Outcomes

  • postoperative exhaust time(within 3 days after operation)

Study Sites (1)

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