MedTrace Logo

Outcomes on Abdominal Versus Vaginal Morcellation At Time of Hysterectomy

NCT04434066 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2024-11-08

No results posted yet for this study

Summary

The purpose of the study is to investigate differences in perioperative and postoperative outcomes between the abdominal (AM) versus vaginal (VM) routes of contained morcellation in participants undergoing laparoscopic total hysterectomies in a randomized controlled trial.

Conditions

  • Abnormal Uterine Bleeding
  • Uterine Bleeding
  • Fibroid Uterus
  • Surgery

Interventions

PROCEDURE

Total Laparoscopic Hysterectomy

Participants will be randomized into either abdominal or vaginal morcellation at time of total laparoscopic hysterectomy

Sponsors & Collaborators

  • University of Texas Southwestern Medical Center

    lead OTHER

Principal Investigators

  • Kimberly A Kho, MD · UT Southwestern Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-01-08
Primary Completion
2022-07-19
Completion
2024-11-05

Countries

  • United States

Study Locations

More Related Trials

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 NCT04434066 on ClinicalTrials.gov