Recruiting

Hip Preservation

Sponsor:

Yale University

Code:

NCT05746533

Conditions

Hip Arthroscopy

Femoroacetabular Impingement

Eligibility Criteria

Sex: All

Age: 12+

Healthy Volunteers: Not accepted

Interventions

Hip Arthroscopy

Study Details

Brief summary:

The purpose of this study is to assess outcomes of hip preservation surgeries including open and arthroscopic treatment of femoroacetabular impingement (FAI).

Conditions

Hip Arthroscopy

Femoroacetabular Impingement

Study ID

NCT05746533

Start date

Jun 2, 2023

Status verified date

May, 2026

Completion date

Jun, 2053

Anticipated

Primary completion date

Jun, 2053

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 12+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Candidates for surgical intervention of the hip
  • Participant and/or guardian has given informed consent and assent as applicable.

Exclusion Criteria:

  • Documented history of pre-existing hip conditions (SCFE, LCPD, acetabular fractures)
  • Has language or cognitive barriers preventing understanding of study and consent and assent documents
  • Prior revision surgeries
  • Patients from the trauma/emergency department
  • Individuals with Unusable x-rays

Study Design

Enrollment

10000 participants

Anticipated

Interventions and Outcome Measures

Arms

Participants Undergoing Hip Preservation/Surgical Interventions

Data will be prospectively collected on participants undergoing hip preservation at Yale-New Haven Hospital.

Interventions

Hip Arthroscopy

Hip Preservation surgeries

Primary outcome measure

  • Change in Hip Outcome Score (iHOT-12) [ Time Frame: Baseline, 3 months post-operatively, 6 months post-operatively, 1 year post-operatively, 2 years post-operatively, 5 years post-operatively, and 10 years post-operatively ]
  • Change in Hip Outcome Score (HOS) [ Time Frame: Baseline, 3 months post-operatively, 6 months post-operatively, 1 year post-operatively, 2 years post-operatively, 5 years post-operatively, and 10 years post-operatively ]
  • Change in PROMIS questionnaire Score [ Time Frame: Baseline, 3 months post-operatively, 6 months post-operatively, 1 year post-operatively, 2 years post-operatively, 5 years post-operatively, and 10 years post-operatively ]
  • Change in Sports Survey Score [ Time Frame: Baseline, 3 months post-operatively, 6 months post-operatively, 1 year post-operatively, 2 years post-operatively, 5 years post-operatively, and 10 years post-operatively ]
  • Change in Pain Score using a visual analog scale (VAS) [ Time Frame: Baseline, 3 months post-operatively, 6 months post-operatively, 1 year post-operatively, 2 years post-operatively, 5 years post-operatively, and 10 years post-operatively ]
  • Change in PROMIS Pain Interference [ Time Frame: Baseline, 3 months post-operatively, 6 months post-operatively, 1 year post-operatively, 2 years post-operatively, 5 years post-operatively, and 10 years post-operatively ]
  • Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Global-10 [ Time Frame: Baseline, 3 months post-operatively, 6 months post-operatively, 1 year post-operatively, 2 years post-operatively, 5 years post-operatively, and 10 years post-operatively ]

Central Contacts and Locations

Central contacts

Andrew Jimenez, MD

813-295-3523andrew.jimenez@yale.edu

Locations

Yale New Haven Health

Recruiting

New Haven, Connecticut, United States, 06520

More Information

Sponsor

Yale University

Last update posted

May 19, 2026

Last verified

May, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Yale University on 2026-05-19.