To evaluate the degree of osteoarthritis 5 to 10 years after a hip arthroscopy in comparison with the non-operative side.
ID
Source
Brief title
Condition
- Joint disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
To evaluate the degree of osteoarthritis 5 to 10 years after a hip arthroscopy
in comparison with the non-operative side.
Secondary outcome
- To evaluate the change in degree of osteoarthritis at 5 to 10 years after a
hip arthroscopy in comparison with preoperative/perioperative.
- To report the incidence of total hip replacement within 5 to 10 years after a
hip arthroscopy. To report the incidence of revision hip arthroscopy within 5
to 10 years after primary hip arthroscopy.
- To determine the functional outcome of patients and, to determine what
factors contribute to a good functional outcome 5/10 years after hip
arthroscopy.
- To determine the inter-rater and intra-rater agreement of the Kellgren and
Lawrence OA score.
- To determine patient satisfaction 5-10 years after hip arthroscopy.
Background summary
A common cause of hip joint pain in the young and active population is
femoroacetabular impingement (FAI) syndrome. If FAI is left untreated, the
changed morphology will have a negative effect on the existing joint and will
contribute to the development of osteoarthritis. Hip arthroscopy is the first
choice of operative treatment for FAI. While hip arthroscopy improves the
patient reported outcome measures (PROMs), the influence of this treatment on
the contribution to the development of osteoarthritis after FAI is to the best
of our knowledge still unknown.
Study objective
To evaluate the degree of osteoarthritis 5 to 10 years after a hip arthroscopy
in comparison with the non-operative side.
Study design
Expansion of a prospective cohort study.
Study burden and risks
All patients will be asked to visit the hospital once. During the visit,
patients will have to complete questionnaires and one radiograph will be made.
Reinier de Graafweg 5
Delft 2625 AD
NL
Reinier de Graafweg 5
Delft 2625 AD
NL
Listed location countries
Age
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
Design
Recruitment
metc-ldd@lumc.nl
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| CCMO | NL86221.058.24 |