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Clinical Trials/NCT01685593
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
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

Sponsor Class
Fed
Responsible Party
Principal Investigator
Principal Investigator

Edward R. Kost, M.D.

Principal Investigator

Brooke Army Medical Center

Study Sites (2)

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