NCT01685593CompletedNot Applicable
A Controlled Randomized Trial Examining the Ability of the Mott Compression Bonder to Decrease Postoperative Pain in Gynecologic Abdominal Laparotomy Patients.
Brooke Army Medical Center2 sites in 1 country76 target enrollmentStarted: January 2001Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Brooke Army Medical Center
- Enrollment
- 76
- Locations
- 2
- Primary Endpoint
- postoperative pain
Study Overview
Brief Summary
We conducted a controlled randomized trial examining the ability of the Mott abdominal Compression Binder to decrease postoperative pain in gynecologic abdominal laparotomy patients
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- Single (Investigator)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •gynecologic abdominal laparotomy patients
Exclusion Criteria
- •non gynecologic abdominal laparotomy patients
Outcomes
Primary Outcomes
postoperative pain
Time Frame: 24 hours
linear pain scale
Secondary Outcomes
- ambulations in 24 hours postoperatively(24 hours)
Investigators
Edward R. Kost, M.D.
Principal Investigator
Brooke Army Medical Center
Study Sites (2)
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