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NCT02249377 · ClinicalTrials.gov registry record · Phase 3

PRP vs Corticosteroid in Baker's Cyst

A Phase 3 study, sponsored by NYU Langone Health.

Terminated
Registry status
Phase 3
Development phase
50
Enrollment target

NCT02249377: Clinical Trial Phase 3 study, sponsored by NYU Langone Health.

NCT02249377 is a Phase 3 study that was terminated before completion, run by NYU Langone Health. The registered enrollment target is 50 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02249377, a Phase 3 study, was terminated before completion, sponsored by NYU Langone Health.

TERMINATED
Registry status
Phase 3
Development phase
50 participants
Enrollment target

Study Summary

This is a Prospective study with Randomized patients into either Ultrasound-guided Platelets-Rich-Plasma injection and Ultrasound guided Corticosteroid Injection, with 3 months and 6 months follow ups after aspiration at our institution. There will be 25 patients in each group, including any patient with symptomatic baker's cyst.

Primary Outcome

Outcome measure will be determined through the use of the Visual Analogue Score (VAS) and the Rauschning and Lindgren criteria which are used to clinically evaluate the presence of the popliteal cysts, pain, posterior sense of tension in the popliteal fossa and its clinical importance for range of motion reduction. The Knee Injury and Osteoarthritis Outcome Score (KOOS) will be used to assess short and long term outcome of knee related conditions.

Interventions

  • DRUG Corticosteroid
  • OTHER Platelets-Rich-Plasma

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2014-02
Est. Completion 2017-04-01
Phase Phase 3
NYU Langone Health

1,164 total trials

Why NCT02249377 stopped before completion

NCT02249377 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 2 interventions - of which Corticosteroid is the first listed.

NCT02249377 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02249377 about?

NCT02249377 is a clinical study titled "PRP vs Corticosteroid in Baker's Cyst". This is a Prospective study with Randomized patients into either Ultrasound-guided Platelets-Rich-Plasma injection and Ultrasound guided Corticosteroid Injection, with 3 months and 6 months follow ups after aspiration at our institution. There will be 25 patients in each group, including any patient...

What is the current status of trial NCT02249377?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 50 participants. The study started on 2014-02. Estimated completion is 2017-04-01.

What interventions are being tested in trial NCT02249377?

The interventions under investigation include: Corticosteroid (DRUG), Platelets-Rich-Plasma (OTHER).

Who is sponsoring clinical trial NCT02249377?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02249377's enrollment target sits among peer trials

50 1844th of 2000 higher than 141 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02249377, the US trial registry maintained by the National Library of Medicine. NCT02249377 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.