Mobius® Post-cesarean Pain Randomized Control Trial

Completed · Not applicable

Conditions studied: Complications; Cesarean Section, Pregnancy

In brief

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.

Key facts

Study ID

NCT00685932

Run by

Abbey Hardy-Fairbanks

People needed

154

Starts

2008-07-01

Expected to finish

2010-06-01

Last updated by the study team

2018-04-18

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Over 18 years old
• Potential for having a cesarean section (scheduled or unscheduled) at Dartmouth Hitchcock Medical Center

You may not qualify if…

• Less than 18 years old
• Unable to consent due to language barrier or psychiatric illness
• Current methadone use for chronic pain
• Stat cesarean section

Where it is running

• Dartmouth-Hitchcock Medical Center — Lebanon, New Hampshire, United States

Full record on ClinicalTrials.gov

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