Abdominal Binder Study to Decrease Postoperative Pain

Postoperative Pain Clinical Trial

Official title:

A Controlled Randomized Trial Examining the Ability of the Mott Compression Bonder to Decrease Postoperative Pain in Gynecologic Abdominal Laparotomy Patients.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01685593
• Other study ID #: C.2001.128
• Status: Completed
• Phase: N/A
• First received: September 12, 2012
• Last updated: September 13, 2012
• Start date: January 2001
• Est. completion date: February 2006

Study information

• Verified date: September 2012
• Source: Brooke Army Medical Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial 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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 76
• Est. completion date: February 2006
• Est. primary completion date: February 2006
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• gynecologic abdominal laparotomy patients

Exclusion Criteria:

• non gynecologic abdominal laparotomy patients

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Pain, Postoperative
• Postoperative Pain

Intervention

Device:
• abdominal binder

Other:
• no binder

Locations

Country	Name	City	State
United States	Brooke Army Medical Center	Ft Sam Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Brooke Army Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	amount morphine used in 24 hours postoperatively	mg morphine	24 hours	No
Primary	postoperative pain	linear pain scale	24 hours	No
Secondary	ambulations in 24 hours postoperatively	number ambulations	24 hours	No