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Completed

NCT Number: NCT01685593

Abdominal Binder Study to Decrease Postoperative Pain

We conducted a controlled randomized trial examining the ability of the Mott abdominal Compression Binder to decrease postoperative pain in gynecologic abdominal laparotomy patients

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Key information

Conditions

Postoperative Pain Neurologic Manifestations Pain Pain, Postoperative Pathologic Processes Pathological Conditions, Signs and Symptoms Postoperative Complications Signs and Symptoms

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Brooke Army Medical Center

Fort Sam Houston, Texas, 78232, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • gynecologic abdominal laparotomy patients

Exclusion criteria

  • non gynecologic abdominal laparotomy patients

Treatment and study plan

Abdominal Binder

Device

no binder

Other

Primary outcomes

  1. postoperative pain

    Time frame: 24 hours

    linear pain scale

Secondary outcomes

  1. ambulations in 24 hours postoperatively

    Time frame: 24 hours

    number ambulations

Other outcomes

  1. amount morphine used in 24 hours postoperatively

    Time frame: 24 hours

    mg morphine

Sponsors and collaborators

Lead sponsor

Brooke Army Medical Center

Fed

Registry information

Official study title

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

Important dates

Study start
2001
Primary completion
2006
Study completion
2006
First posted
Sep 14, 2012
Registry last updated
Sep 14, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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