CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 285 enrolled
Drug / intervention
Enrollment video +4 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01166373
NCT01166373N/ACompleted

Long-Term Effectiveness Of Sacrospinous Ligament Fixation vs Uterosacral Ligament Suspension With and Without Perioperative Behavioral Therapy/Pelvic Muscle Training: Extended Operations & Pelvic Muscle Training Of Apical Support Loss Study

NICHD Pelvic Floor Disorders Network·interventional·Posted Jul 21, 2010·Updated Sep 28, 2020

In Brief

A clinical study evaluating Enrollment video, SSLF, and 3 other interventions for Pelvic Organ Prolapse. Completed, enrolled 285 participants across 7 sites.

Detailed Summary

Women will be invited to participate in E-OPTIMAL at their last clinical follow-up visit for OPTIMAL (at 24 months post surgery). E-OPTIMAL is an extension of the ongoing OPTIMAL study and no new study treatment interventions will be given. Rather an enrollment intervention will be investigated with potential E-OPTIMAL participants randomly assigned to watch a standardized video prior to consent or undergo the standard informed consent process. The standardized video will review the rationale for women's health research, the importance of long-term follow-up and a detailed invitation to participate in E-OPTIMAL. The video has undergone review by potential subjects, coordinators and physician researchers to ensure that the relevance and importance of issues potentially impacting on long-term participation in studies such as E-OPTIMAL are covered. Participation in E-OPTIMAL will occur up to three additional years. Women will be strongly encouraged to participate in annual examinations and annual telephone surveys but may participate in only one of these study parts if needed. We propose to test the following null hypotheses: 1. There will be no difference in time to surgical failure between uterosacral vaginal vault ligament suspension (ULS) and sacrospinous ligament fixation (SSLF) up to 5 years after surgery. 2. The addition of a standardized video detailing the importance of long-term follow-up studies for POP to the informed consent process will not improve enrollment or retention in E-OPTIMAL.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedJul 21, 2010
Enrollment StartApr 1, 2010
Primary CompletionJul 1, 2016
TodayJul 2, 2026
Enrollment to primary: 6.3 yearsPosted 15.9 years ago

Interventions

Enrollment videobehavioral

Standardized video detailing the importance of long-term follow-up studies for pelvic organ prolapse prior to the informed consent process

SSLFprocedure

sacrospinous ligament fixation to suspend the vaginal apex

ULSprocedure

uterosacral ligament suspension to suspend the vaginal apex

PMTbehavioral

perioperative behavioral therapy / pelvic muscle training with formal individualized PMT program that begins two to four weeks prior to surgery and continues for three months after surgery

Usual Careother

usual care both before and after prolapse surgery with respect to pelvic muscle training