MedTrace Logo

Long Term Outcomes Following Total Laparoscopic Hysterectomy and Laparoscopic Supracervical Hysterectomy

NCT01289314 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2011-02-10

No results posted yet for this study

Summary

Objective: To compare the occurrence and intensity of pelvic pain as well as patient satisfaction and quality of life after total laparoscopic and laparoscopic supracervical hysterectomy.

Design: Prospective randomised trial.

Null hypothesis 1: There is no significant difference in occurrence and intensity of pelvic pain following TLH compared with following LSH.

Null hypothesis 2: There is no significant difference in patient satisfaction and quality of life following TLH compared with following LSH.

Conditions

  • Total Laparoscopic Hysterectomy
  • Laparoscopic Supracervical Hysterectomy
  • Fibromas
  • Abnormal Uterine Bleeding
  • Dysmenorrhea

Interventions

PROCEDURE

TLH

Total laparoscopic hysterectomy (TLH)

PROCEDURE

Laparoscopic supracervical hysterectomy

Laparoscopic supracervical hysterectomy (LSH)

Sponsors & Collaborators

  • Oslo University Hospital

    lead OTHER

Principal Investigators

  • Marit Lieng, MD PHD · Dept. of Gynecology, Oslo University Hospital, Norway

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2011-12-31
Completion
2012-12-31

Countries

  • Norway

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 NCT01289314 on ClinicalTrials.gov