Long Term Results After Hip Arthroscopy

NCT ID: NCT06327217

Last Updated: 2024-03-25

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Total Enrollment: 451 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-04-01
• Study Completion Date: 2025-03-01

Brief 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 (OA). 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.

Conditions

Femoro Acetabular Impingement

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Hip arthroscopy 5-10jr

Bilateral hip x-ray

Intervention Type: RADIATION

Patients will be asked to visit the clinic for a bilateral hip x-ray, in order to evaluate the degree os osteoarthritis.

Questionnaires

Intervention Type: OTHER

Patients will be asked to complete questionnaires on function, quality of life and pain (the modified Harris Hip Score (mHHS), Hip Outcome Score (HOS), the World Health Organisation Quality of Life Questionnaire (WHOWOL) and Visual Analogue Scale (VAS) for pain). One question will be asked: 'How satisfied are you with the results of the surgery?' on a 10-point scale.

Interventions

Bilateral hip x-ray

Patients will be asked to visit the clinic for a bilateral hip x-ray, in order to evaluate the degree os osteoarthritis.

Intervention Type: RADIATION

Questionnaires

Patients will be asked to complete questionnaires on function, quality of life and pain (the modified Harris Hip Score (mHHS), Hip Outcome Score (HOS), the World Health Organisation Quality of Life Questionnaire (WHOWOL) and Visual Analogue Scale (VAS) for pain). One question will be asked: 'How satisfied are you with the results of the surgery?' on a 10-point scale.

Intervention Type: OTHER

Eligibility Criteria

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.

A potential subject who meets any of the following criteria will be excluded from participation in this study:

Exclusion Criteria

• Patient who has had hip arthroscopy of both sides;
• Patient is unable or unwilling to sing informed consent

• Minimum Eligible Age: 16 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Reinier Haga Orthopedisch Centrum

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Reinier Haga Orthopedic Center

Zoetermeer, , Netherlands

Countries

Netherlands

Other Identifiers

OC-2023-009

Identifier Type: -

Identifier Source: org_study_id