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Study of Laparoendoscopic Single Site Hysterectomy in Benign and Preinvasive Uterine Disease

NCT01679548 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 424

Last updated 2024-03-25

No results posted yet for this study

Summary

To compare the efficacy between single-port and three-port laparoscopic assisted vaginal hysterectomy in patients with benign or preinvasive uterine disease

Conditions

  • Benign or Preinvasive Uterine Disease

Interventions

PROCEDURE

Single-port LAVH

LESS LAVH was performed using a commercially available four-channel, single-port system. A rigid, 0-degree, 5 mm laparoscope was used.

PROCEDURE

Three-port LAVH

Conventional LAVH was performed using three ports; a 12, 10, and 5-mm port was placed in the umbilicus, left lower quadrant, and suprapubic area, respectively. A rigid, 0-degree, 12 mm laparoscope was introduced through 12mm port of umbilicus.

Sponsors & Collaborators

  • Asan Medical Center

    lead OTHER

Principal Investigators

  • Joo-Hyun Nam, M.D., Ph.D. · Asan Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-11-23
Primary Completion
2018-12-12
Completion
2019-06-11

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01679548 on ClinicalTrials.gov