Outcome After Arthroscopic Surgery in Patients Treated With PAO
Outcome After Arthroscopic Labrum Surgery in Patients Treated With Periacetabular Osteotomy
1 other identifier
observational
45
0 countries
N/A
Brief Summary
The purpose of the study is to evaluate outcome after arthroscopy if the hip in patients previous treated with periacetabular osteotomy
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2015
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2015
CompletedFirst Submitted
Initial submission to the registry
March 18, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2016
CompletedFirst Posted
Study publicly available on registry
October 26, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2016
CompletedFebruary 23, 2017
October 1, 2016
1.8 years
March 18, 2015
February 21, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
Number of patient with the need of a total hip arthroplasty after PAO and hip arthroscopy
Questionnaire
48 months after hip arthroscopy
Secondary Outcomes (3)
Evaluation of the patients pain in rest and during activity on a NRS Scale
48 months after hip arthroscopy
Evaluation of hip function and pain using MHHS (modified harris hip score)
48 months after hip arthroscopy
Evaluation of hip function and pain using HOS (Hip outcome score)
48 months after hip arthroscopy
Interventions
Follow up after hip arthroscopy in pt with previous PAO. Follow up by questionnaires send til the cohort
Eligibility Criteria
Patients undergoing hip arthrocopy previous treated with periacetabular osteotomy
You may qualify if:
- previous PAO and hip arthroscopy
- developmental dysplasia of the hip
You may not qualify if:
- calve legg perthes disease
- femoral osteotomy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Martin Lind, MD,PhD,DmSc
Aarhus University Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
March 18, 2015
First Posted
October 26, 2016
Study Start
January 1, 2015
Primary Completion
October 1, 2016
Study Completion
December 1, 2016
Last Updated
February 23, 2017
Record last verified: 2016-10