ong term results after hip arthoscopy
Not yet recruiting
- Conditions
- hip arthroscopyosteoarthritis10023213
- Registration Number
- NL-OMON56691
- Lead Sponsor
- Reinier de Graaf Groep
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 451
Inclusion Criteria
- Patient who participated in the cohort study;
- At least 5 years of follow up;
- Patient is able to understand the meaning of the study and is willing to sign
the Informed Consent Form.
Exclusion Criteria
- Patient who has had hip arthroscopy of both sides;
- Patient is unable or unwilling to sign informed consent.
- Patient who is pregnant
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>To evaluate the degree of osteoarthritis 5 to 10 years after a hip arthroscopy<br /><br>in comparison with the non-operative side. </p><br>
- Secondary Outcome Measures
Name Time Method <p>- To evaluate the change in degree of osteoarthritis at 5 to 10 years after a<br /><br>hip arthroscopy in comparison with preoperative/perioperative.<br /><br>- To report the incidence of total hip replacement within 5 to 10 years after a<br /><br>hip arthroscopy. To report the incidence of revision hip arthroscopy within 5<br /><br>to 10 years after primary hip arthroscopy.<br /><br>- To determine the functional outcome of patients and, to determine what<br /><br>factors contribute to a good functional outcome 5/10 years after hip<br /><br>arthroscopy.<br /><br>- To determine the inter-rater and intra-rater agreement of the Kellgren and<br /><br>Lawrence OA score.<br /><br>- To determine patient satisfaction 5-10 years after hip arthroscopy. </p><br>