NCT02204514

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
62

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Apr 2014

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2014

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

July 25, 2014

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 30, 2014

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2014

Completed
Last Updated

October 20, 2015

Status Verified

October 1, 2015

Enrollment Period

5 months

First QC Date

July 25, 2014

Last Update Submit

October 16, 2015

Conditions

Hip Pain

Outcome Measures

Primary Outcomes (1)

  • Self-reported pain

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

    1-6 years after surgery

Study Arms (1)

Surgery for external snapping hip

Procedure: Surgery for external snapping hip

Interventions

Surgery for external snapping hipPROCEDURE
Surgery for external snapping hip

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients undergoing surgery for painful external snapping hip in The North Denmark Region between 2008-2013 with at least 1 year follow-up time.

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Orthopedic Surgery

Aalborg, 9000, Denmark

Location

MeSH Terms

Interventions

Surgical Procedures, Operative

Study Officials

  • Søren T Skou, PT, MSc

    Orthopedic Surgery Research Unit + Department of Health Science and Technology, Aalborg University

    PRINCIPAL INVESTIGATOR

  • Stine Jorstad, BSc

    Department of Orthopedic Surgery

    STUDY CHAIR

  • Ole Simonsen, MD, DMSc

    Department of Orthopedic Surgery

    STUDY CHAIR

  • Anders C Laursen, MD

    Department of Orthopedic Surgery

    STUDY CHAIR

  • Michael Ulrich, MD, PhD, DMSc

    Department of Orthopedic Surgery

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD, DMSc

Study Record Dates

First Submitted

July 25, 2014

First Posted

July 30, 2014

Study Start

April 1, 2014

Primary Completion

September 1, 2014

Study Completion

September 1, 2014

Last Updated

October 20, 2015

Record last verified: 2015-10

Locations

DK(1)