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Completed

NCT Number: NCT03407612

Outcomes of CPM Usage Following Arthroscopic Acetabular Labral Repair

The purpose of this study is to measure whether CPM (continuous passive motion) usage improves outcomes following arthroscopic hip surgery that includes labral repair. Investigators tested the hypothesis that CPM usage reduces pain levels and pain medication use and improves function in individuals who undergo hip arthroscopy.

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Key information

Conditions

Femoro Acetabular Impingement Femoracetabular Impingement Hip Labral Tear Joint Diseases Musculoskeletal Diseases Neurologic Manifestations Pain Pain, Postoperative Pathologic Processes Pathological Conditions, Signs and Symptoms Postoperative Complications Signs and Symptoms

Age range

14 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Ohio State University Wexner Medical Center

Columbus, Ohio, 43212, United States

About this study

Subjects undergoing primary hip arthroscopy for acetabular labral repair were randomized to determine whether they would receive a CPM. Those subjects receiving a CPM were instructed to use it for 4-6 hours daily throughout the first two postoperative weeks. The total number of pain medications and average pain scores over the two weeks, as well as Hip Outcome Score Activity of Daily Living (HOS ADL) scores at standard time points were compared via a two sample t-test and intention-to-treat analysis.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • undergoing hip arthroscopy to repair a torn labrum

Exclusion criteria

  • pregnancy
  • revision surgery
  • bilateral surgery

Treatment and study plan

Continuous Passive Motion

Device

CPM devices are used in postoperative rehabilitation and are throughout to reduce joint stiffness.

Primary outcomes

  1. Change in Patient Satisfaction and Functional Outcome

    Time frame: Baseline and 6 weeks, 12 weeks, and 6 months postoperatively

    Hip Outcome Score Activities of Daily Living (HOS ADL) questionnaire completed at specific time points. Completion of the HOS ADL provides a score from 0 to 100, with a higher score corresponding to greater level of function. The improvement preoperative to 6 month postoperative scores was also computed.

Secondary outcomes

  1. Analgesic Usage

    Time frame: Initial two postoperative weeks

    Analgesic usage measured via the morphine-equivalent dose of consumed analgesic medications

  2. Pain Level

    Time frame: Initial two postoperative weeks

    Change in pain level measured on a Likert-type scale from 0 to 10, with higher scores representing higher pain levels.

Sponsors and collaborators

Lead sponsor

Ohio State University

Other

Registry information

Official study title

The Effect of Continuous Passive Motion on Pain Control Following Hip Arthroscopy

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Jan 23, 2018
Registry last updated
Oct 8, 2020

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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