CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 54 enrolled
Drug / intervention
VCE +1 moreother
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/NCT04138810
NCT04138810N/ACompleted
CompareCT.gov

Assessment of Video-conference Technology for Post-operative Follow up in a Urogynecologic Population

University of Pennsylvania·interventional·Posted Oct 25, 2019·Updated Aug 24, 2020

In Brief

A clinical study evaluating VCE and Survey for Pelvic Organ Prolapse. Completed, enrolled 54 participants across 1 site.

Detailed Summary

Postoperative follow up is necessary following any surgical procedure and has been conducted in the same manner since the field of surgery began. The study will determine feasibility and patient satisfaction of innovative postoperative virtual clinical encounters utilizing mobile video conference technology for women undergoing pelvic reconstructive surgery through a randomized controlled trial.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPelvic Organ Prolapse
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedOct 25, 2019
Enrollment StartJul 17, 2017
Primary CompletionJul 1, 2019
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 6.7 years ago

Interventions

VCEother

Videoconference conducted according to a standard script which reviews the following key aspects of post-operative care: bowel functions, voiding functions, presence of vaginal bleeding, pain control, diet status, ambulatory status and any additional concerns. Standard post-operative instructions and precautions are reviewed as well.

Surveyother

Measure of satisfaction regarding post-op visit.