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Clinical Trials/NCT02204514
NCT02204514CompletedNot Applicable

The Effects of Surgery for Painful External Snapping Hip

Northern Orthopaedic Division, Denmark1 site in 1 country62 target enrollmentStarted: April 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
62
Locations
1
Primary Endpoint
Self-reported pain

Study Overview

Brief Summary

The purpose of this study is to assess the pain-relieving effects of surgery for painful external snapping hip.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients undergoing surgery for painful external snapping hip
  • •18 years or older

Exclusion Criteria

  • •Inability to comply with the protocol (e.g. due to dementia)

Outcomes

Primary Outcomes

Self-reported pain

Time Frame: 1-6 years after surgery

Do you still have the same pain as before surgery? Response categories: yes; no

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Northern Orthopaedic Division, Denmark
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ole Simonsen

MD, DMSc

Northern Orthopaedic Division, Denmark

Study Sites (1)

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