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Could your own blood ease hip pain? PRP injection shows promise

NCT ID NCT06332352

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether a single injection of platelet-rich plasma (PRP) into the hip joint can relieve pain and improve function in people with a torn hip labrum. Thirty adults aged 18 to 49 who had not improved with standard care received the injection. Researchers tracked their pain, hip function, and overall health using surveys over six months.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
platelet-rich plasma (PRP)
What this could lead to
If it works, this could offer a non-surgical option to reduce hip pain and improve daily function for people with labral tears.
What could go wrong
This is a small, completed study with only 30 participants and no comparison group, so results may not apply widely. PRP injections can cause temporary pain or swelling.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

30 people

The number who actually took part.

Started

Mar 2024

Finished

Mar 2026

Lead sponsor

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.

Ages

18 to 49 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: * Age ≤49 years old (i.e., 18 - 49 years old) * Hip or groin pain with at least 1 positive provocative labral hip maneuver (i.e., Flexion, Adduction, Internal Rotation (FADIR) test, subspine impingement test, scour) * Radiographs with Tonnis grade \< 2 (i.e., 0 or 1) * MRI or MRA hip with evidence of acetabular labral tear * Failure of at least 6 weeks of conservative management \[i.e., activity modification, non-steroidal anti-inflammatory drugs (NSAIDs), and/or physical therapy (PT), other intra-articular injection etc.\] * Prior diagnostic ultrasound guided hip injection with anesthetic-only providing ≥50% pain relief Exclusion Criteria: * Any prior surgery to the affected hip * Imaging with evidence of avascular necrosis of the affected hip * Imaging with evidence of hip dysplasia (i.e. lateral center edge angle of ≤20 degrees) * Alpha angle of ≥55 degrees of the affected hip * Intra-articular hip injection within the last 6 months to the affected hip of any injectate with the exception of anesthetic * Active systemic infection requiring antibiotics or local infection at the site of the injection * Any prior intra-articular infection of the affected hip * Any prior fracture of the affected femur or pelvis * Blood dyscrasia or malignancy * Non-ambulatory patients * Patient seeking care with active litigation pending * Body mass index (BMI) ≥ 35 kg/m2 * Systemic inflammatory arthropathy * Oral steroids consumed within the last three months

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • University of Utah - Department of Orthopaedics

    Salt Lake City, Utah, 84108, United States

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