Trials / Completed
CompletedNCT01685593
Abdominal Binder Study to Decrease Postoperative Pain
A Controlled Randomized Trial Examining the Ability of the Mott Compression Bonder to Decrease Postoperative Pain in Gynecologic Abdominal Laparotomy Patients.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 76 (actual)
- Sponsor
- Brooke Army Medical Center · Federal
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | abdominal binder | |
| OTHER | no binder |
Timeline
- Start date
- 2001-01-01
- Primary completion
- 2006-02-01
- Completion
- 2006-02-01
- First posted
- 2012-09-14
- Last updated
- 2012-09-14
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01685593. Inclusion in this directory is not an endorsement.