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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
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01685593
Enrollment
76
Registered
2012-09-14
Start date
2001-01-31
Completion date
2006-02-28
Last updated
2012-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Keywords

abdominal binder

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

Interventions

DEVICEabdominal binder
OTHERno binder

Sponsors

Brooke Army Medical Center
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* gynecologic abdominal laparotomy patients

Exclusion criteria

* non gynecologic abdominal laparotomy patients

Design outcomes

Primary

MeasureTime frameDescription
postoperative pain24 hourslinear pain scale

Secondary

MeasureTime frameDescription
ambulations in 24 hours postoperatively24 hoursnumber ambulations

Other

MeasureTime frameDescription
amount morphine used in 24 hours postoperatively24 hoursmg morphine

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026