Ignite Creation Date:
2024-05-06 @ 10:59 AM
Last Modification Date:
2024-10-26 @ 12:38 PM
Study NCT ID:
NCT03407612
Status:
COMPLETED
Last Update Posted:
2020-10-08
First Post:
2018-01-09
Brief Title:
Outcomes of CPM Usage Following Arthroscopic Acetabular Labral Repair
Sponsor:
Ohio State University
Organization:
Ohio State University
Study Overview
Official Title:
The Effect of Continuous Passive Motion on Pain Control Following Hip Arthroscopy
Status:
COMPLETED
Status Verified Date:
2020-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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
Detailed 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None