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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06047730

Enrollment

173

Registered

2023-09-21

Start date

2017-01-01

Completion date

2023-03-31

Last updated

2023-09-21

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

Conditions

Laparoscope, Malignant Ovarian Tumor, Single-site Surgery

Keywords

Transumbilical laparoendoscopic single-site surgery,Giant malignant ovarian tumor

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.

Interventions

PROCEDUREoperation ways

nothing

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

10 Years to 80 Years

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame	Description
peroperative bleeding	during the operation time	peroperative bleeding

Secondary

Measure	Time frame	Description
postoperative exhaust time	within 3 days after operation	postoperative exhaust time

Countries

China

Outcome results

None listed

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