Researchers track hip motion to uncover impingement secrets
NCT ID NCT01575964
First seen Jun 27, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This study looks at how a hip condition called femoroacetabular impingement (FAI) changes the way the hip joint moves. Researchers will compare 36 people with FAI to those without it. The goal is to better understand the mechanics behind the condition, which may help improve future treatments.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 36 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Jan 2012
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Normal subjects and subjects with femoroacetabular impingement.
- Ages
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18 to 35 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients who present with hip pain subsequently diagnosed as femoroacetabular impingement * Subjects who meet the following radiographic criterion of cam or pincer FAI, will be given the opportunity to volunteer in this study. * Subjects that demonstrate a cross-over-sign or a lateral center edge angle (LCEA) without an alpha angle, will be classified as having pincer FAI. * Subjects with an alpha angle, without a cross-over sign or LCEA, will be categorized as having cam type FAI. * Finally, with at least one cam (alpha angle) and pincer sign "cross-over-sign or a lateral center edge angle (LCEA)" will be classified as mixed FAI. Control Population Inclusion Criteria: * 12 controls will consist of volunteers in the same age range as the subject groups (18-35 years). * Control hips will be screened with a standard AP radiograph. Normal volunteers who have radiographic evidence of FAI, dysplasia or other joint deformities will be excluded. Exclusion Criteria: * Subjects who have radiographic evidence of osteoarthritis (Tonnis Grade III or IV) will be excluded as this study focuses on the mechanics of hips before prominent cartilage damage. * Subjects who have had prior procedures to correct FAI or other hip conditions will be excluded (exploratory procedures will be included). * Minors (under age 18), mentally disabled, persons incarcerated, on parole, probation awaiting trial, or pregnant women are excluded from this study. * A human Chorionic Gondaotropin (hCG) urine pregnancy test will be performed on all women prior to the study. * To limit the annual radiation exposure to any participating volunteers, we will exclude anyone who has had a CT scan or participated in a research study involving ionizing radiation in the past 12 months. Motion Capture Exclusion Criteria: * Subjects who are unwilling or unable to perform the proposed activities of daily living or undergo the clinical exams will be dismissed. * Subjects with a BMI less than 30 (www.nhlbisupport.com/bmi/) or those with dense hip musculature/wide hips (maximum of 42 cm of circumferential hip length) will be excluded. CT Exclusion Criteria: * Subjects who are unwilling or unable to remain still. * Subjects who are allergic to contrast agent and/or lidocaine will be dismissed.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Utah Orthopaedic Center
Salt Lake City, Utah, 84108, United States
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