Hip Labral Tear Clinical Trial
Official title:
Study of RNS60 on Post-operative Pain and Function in Patients Undergoing Hip Labral Repair or Reconstruction Surgery
NCT number | NCT02005523 |
Other study ID # | 07.1.1.H2 |
Secondary ID | |
Status | Withdrawn |
Phase | Phase 2 |
First received | December 3, 2013 |
Last updated | February 4, 2015 |
Verified date | February 2015 |
Source | Revalesio Corporation |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Interventional |
The purpose of this study is to see if use of RNS60 during hip labral repair surgery decreases pain and improves functional capacity post-operation.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | October 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Revalesio Corporation |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Assessment of post-operative pain | Comparison of scores from validated pain scales from post-surgery to one week. | 1 week | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03407612 -
Outcomes of CPM Usage Following Arthroscopic Acetabular Labral Repair
|
N/A |