Trial Outcomes & Findings for Intra-articular Platelet-Rich Plasma for Acetabular Labral Tears (NCT NCT06332352)
NCT ID: NCT06332352
Last Updated: 2026-06-25
Results Overview
Global patient satisfaction was assessed prospectively at 6 months following the intervention using a numeric rating scale ranging from 0 to 100. Participants were asked to rate their hip, where 0 represented "worst possible" and 100 represented "best possible." The score reflects the participant's overall perception of their injection, including symptom improvement and overall experience.
COMPLETED
NA
30 participants
6 Months
2026-06-25
Participant Flow
Patients were recruited from March through December 2024. Patients were clinically diagnosed with a symptomatic acetabular labral tear by a primary care or orthopedic sports medicine physician in a tertiary outpatient, orthopedic clinic setting. Patients who met inclusion criteria were referred to the study and given the option of participation.
This was an open-label study; therefore, no randomization was performed. In some cases, participants had more than one hip enrolled, accounting for the difference between the number of participants (n=28) and the number of units/hips enrolled (n=30).
Unit of analysis: Hips
Participant milestones
| Measure |
Intra-Articular Hip Injection of PRP
Single Group Assignment Recruitment will occur at the University of Utah Orthopedic Center by physician and study staff members medical chart review before patient visits. 45 mL of blood will be collected from eligible participants and processed. A single processed neutrophil-poor PRP injection will be given once to a single hip.
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|---|---|
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Overall Study
STARTED
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28 30
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Overall Study
COMPLETED
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28 30
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Overall Study
NOT COMPLETED
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0 0
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Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Some participants had two different hips enrolled in the study, which explains the difference between the number of participants and the number of hips (units) analyzed.
Baseline characteristics by cohort
| Measure |
Intra-Articular Hip Injection of PRP
n=30 Hips
Single Group Assignment Recruitment will occur at the University of Utah Orthopedic Center by physician and study staff members medical chart review before patient visits. 45 mL of blood will be collected from eligible participants and processed. A single processed neutrophil-poor PRP injection will be given once to a single hip.
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|---|---|
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Age, Continuous
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37 Years
n=28 Participants • Some participants had two different hips enrolled in the study, which explains the difference between the number of participants and the number of hips (units) analyzed.
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Sex: Female, Male
Female
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19 Participants
n=28 Participants • Some participants had two different hips enrolled in the study, which explains the difference between the number of participants and the number of hips (units) analyzed.
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Sex: Female, Male
Male
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9 Participants
n=28 Participants • Some participants had two different hips enrolled in the study, which explains the difference between the number of participants and the number of hips (units) analyzed.
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BMI
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24 kg/m^2
n=28 Participants • Some participants had two different hips enrolled in the study, which explains the difference between the number of participants and the number of hips (units) analyzed.
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Duration of symptoms
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12 Months
n=28 Participants • Some participants had two different hips enrolled in the study, which explains the difference between the number of participants and the number of hips (units) analyzed.
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Global Assessment Score
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51 score on a scale
n=30 Hips
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International Hip Outcome Tool (iHOT-12)
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50.5 score on a scale
n=30 Hips
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EQ VAS (EuroQual Visual Analog Scale)
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68 score on a scale
n=30 Hips
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PRIMARY outcome
Timeframe: 6 MonthsPopulation: Some participants had two different hips enrolled in the study, which explains the difference between the number of participants and the number of hips (units) analyzed.
Global patient satisfaction was assessed prospectively at 6 months following the intervention using a numeric rating scale ranging from 0 to 100. Participants were asked to rate their hip, where 0 represented "worst possible" and 100 represented "best possible." The score reflects the participant's overall perception of their injection, including symptom improvement and overall experience.
Outcome measures
| Measure |
Intra-Articular Hip Injection of PRP
n=30 Hips
Single Group Assignment Recruitment will occur at the University of Utah Orthopedic Center by physician and study staff members medical chart review before patient visits. 45 mL of blood will be collected from eligible participants and processed. A single processed neutrophil-poor PRP injection will be given once to a single hip.
|
|---|---|
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Global Assessment Score
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75 score on a scale
Interval 60.3 to 87.3
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PRIMARY outcome
Timeframe: 6 MonthsPopulation: Some participants had two different hips enrolled in the study, which explains the difference between the number of participants and the number of hips (units) analyzed.
Description: The International Hip Outcome Tool-12 (iHOT-12) is a validated, patient-reported outcome measure designed to assess symptoms, functional limitations, and quality of life in young, active individuals with hip disorders. Structure: The iHOT-12 consists of 12 items that capture four domains: Symptoms and Functional Limitations Sports and Recreational Activities Job-Related Concerns Social, Emotional, and Lifestyle Concerns Each item is presented as a visual analog scale (VAS). Scoring: Each item is scored from 0 to 100. 0 = severe symptoms/extreme limitations 100 = no symptoms/no limitations The overall score is calculated as the mean of all answered items (range 0-100), with higher scores indicating better hip function and quality of life.
Outcome measures
| Measure |
Intra-Articular Hip Injection of PRP
n=30 Hips
Single Group Assignment Recruitment will occur at the University of Utah Orthopedic Center by physician and study staff members medical chart review before patient visits. 45 mL of blood will be collected from eligible participants and processed. A single processed neutrophil-poor PRP injection will be given once to a single hip.
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|---|---|
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International Hip Outcome Tool (iHOT-12)
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75.9 Scores on a scale
Interval 68.1 to 87.1
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PRIMARY outcome
Timeframe: 6 MonthsPopulation: Some participants had two different hips enrolled in the study, which explains the difference between the number of participants and the number of hips (units) analyzed.
The EQ Visual Analog Scale (EQ VAS) was used to assess participants' self-rated overall health at the primary end-point. Participants rated their health on a scale from 0 to 100, where 0 represents the worst imaginable health and 100 represents the best imaginable health. Higher scores indicate better perceived health status.
Outcome measures
| Measure |
Intra-Articular Hip Injection of PRP
n=30 Hips
Single Group Assignment Recruitment will occur at the University of Utah Orthopedic Center by physician and study staff members medical chart review before patient visits. 45 mL of blood will be collected from eligible participants and processed. A single processed neutrophil-poor PRP injection will be given once to a single hip.
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|---|---|
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EQ VAS (EuroQual Visual Analog Scale)
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77.5 Scores on a scale
Interval 68.7 to 86.5
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Adverse Events
Intra-Articular Hip Injection of PRP
Serious adverse events
Adverse event data not reported
Other adverse events
| Measure |
Intra-Articular Hip Injection of PRP
n=28 participants at risk
Single Group Assignment Recruitment will occur at the University of Utah Orthopedic Center by physician and study staff members medical chart review before patient visits. 45 mL of blood will be collected from eligible participants and processed. A single processed neutrophil-poor PRP injection will be given once to a single hip.
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|---|---|
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Musculoskeletal and connective tissue disorders
Increase pain in the hip
|
53.6%
15/28 • From enrollment until the end of follow-up, up to one month
Twenty-eight participants were at risk of an adverse event. However since some participants (n=2) had both hips enrolled in the study, there is a difference between the number of participants (n=28) and the number of hips (n=30) analyzed.
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Musculoskeletal and connective tissue disorders
Reduced hip range of motion
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35.7%
10/28 • From enrollment until the end of follow-up, up to one month
Twenty-eight participants were at risk of an adverse event. However since some participants (n=2) had both hips enrolled in the study, there is a difference between the number of participants (n=28) and the number of hips (n=30) analyzed.
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Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place