CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 154 enrolled
Drug / intervention
Mobius Retractordevice
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/NCT00685932
NCT00685932N/ACompleted
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Mobius Pain Study: A Randomized Controlled Trial of Standard Versus Mobius® Retraction at Cesarean Delivery

Abbey Hardy-Fairbanks·interventional·Posted May 29, 2008·Updated Apr 18, 2018

In Brief

A clinical study evaluating Mobius Retractor for Complications; Cesarean Section and Pregnancy. Completed, enrolled 154 participants across 1 site.

Detailed Summary

The purpose of this study is to investigate whether the use of the Mobius® retractor decreased post-operative pain after cesarean section verses conventional retractor use. Based on clinical experience and a pilot study, we suspect that the retractor will decrease overall pain as well as lateral pain.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsComplications; Cesarean Section, Pregnancy
CountriesUnited States
CollaboratorsApple Medical Corporation

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 29, 2008
Enrollment StartJul 1, 2008
Primary CompletionJun 1, 2010
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 18.1 years ago

Interventions

Mobius Retractordevice

The Mobius retractor is a dual ring elastic self retaining retractor that is inserted into the abdominal cavity after the peritoneal incision has been established. It is then left in place during the hysterotomy incision, delivery of the fetus, hysterotomy repair, inspection and irrigation.