ClinicalTrials.Veeva

Menu

Outcomes of CPM Usage Following Arthroscopic Acetabular Labral Repair

The Ohio State University logo

The Ohio State University

Status

Completed

Conditions

Femoro Acetabular Impingement
Hip Labral Tear
Pain, Postoperative

Treatments

Device: Continuous Passive Motion

Study type

Interventional

Funder types

Other

Identifiers

NCT03407612
2011H0416

Details and patient eligibility

About

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.

Full description

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.

Enrollment

54 patients

Sex

All

Ages

14 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • undergoing hip arthroscopy to repair a torn labrum

Exclusion criteria

  • pregnancy
  • revision surgery
  • bilateral surgery

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

54 participants in 2 patient groups

CPM
Active Comparator group
Description:
These subjects received a continuous passive motion (CPM) device and were instructed to use it for 4-6 hours daily throughout the first two postoperative weeks following their arthroscopic labral repair. They were provided adequate education on how to operate the device. The subjects recorded their average usage of the CPM, as well as their personal perception of the CPM, at the postoperative 2 day, 7 day, and 14 day marks.
Treatment:
Device: Continuous Passive Motion
No CPM
No Intervention group
Description:
No CPM was administered to these subjects.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems