Abdominal Binder Study to Decrease Postoperative Pain

Completed · Not applicable

Conditions studied: Postoperative Pain

In brief

We conducted a controlled randomized trial examining the ability of the Mott abdominal Compression Binder to decrease postoperative pain in gynecologic abdominal laparotomy patients

Key facts

Study ID

NCT01685593

Run by

Brooke Army Medical Center

People needed

76

Starts

2001-01-01

Expected to finish

2006-02-01

Last updated by the study team

2012-09-14

Who can join

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

You may qualify if…

• gynecologic abdominal laparotomy patients

You may not qualify if…

• non gynecologic abdominal laparotomy patients

Where it is running

• Brooke Army Medical Center — Fort Sam Houston, Texas, United States

Full record on ClinicalTrials.gov

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