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ACTIVE NOT RECRUITING NA

HyaloFAST Trial for Repair of Articular Cartilage in the Knee

NCT02659215 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the safety and efficacy of Hyalofast® scaffold with bone marrow aspirate concentrate (BMAC) compared to microfracture in the treatment of symptomatic cartilage defects of the knee.

Interventions

  • PROCEDURE Microfracture
  • DEVICE Hyalofast

Study Locations (20)

California

  • Axis Clinical Trials — Los Angeles
  • Kerlan-Jobe Orthopedic Clinic — Los Angeles
  • BioSolutions Clinical Research Center — San Diego
  • New Hope Research Development — Tarzana

Florida

  • Paramount Trials, LLC — Miami
  • Suncoast Clinical Research — New Port Richey

Louisiana

  • Bone and Joint Clinic of Baton Rouge — Baton Rouge
  • Covington Orthopedic and Sports Medicine Institute — Covington

Texas

  • Austin Ortho Biologics / Seton Medical Center Austin — Austin
  • Baylor Scott & White — Temple

Arizona

  • Physicians Research Group — Tempe

Connecticut

  • Orthopedic Foundation — Stamford

Illinois

  • OrthoIllinois — Rockford

Nevada

  • Clinical Research Center of Nevada — Las Vegas

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2015-12
Est. Completion 2026-06-30
Phase NA

Sponsor

Anika Therapeutics

30 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02659215

The ClinicalTrials.gov registry entry for NCT02659215 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Anika Therapeutics, which has 30 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Defect of Articular Cartilage appearing as the primary indexed condition, and to 2 interventions — of which Microfracture is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02659215 reports 20 study locations spanning 14 distinct geographic areas — top geographies include California, Florida, Louisiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02659215 about?

NCT02659215 is a clinical study titled "HyaloFAST Trial for Repair of Articular Cartilage in the Knee". The purpose of this study is to evaluate the safety and efficacy of Hyalofast® scaffold with bone marrow aspirate concentrate (BMAC) compared to microfracture in the treatment of symptomatic cartilage defects of the knee.

What is the current status of trial NCT02659215?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2015-12. Estimated completion is 2026-06-30.

What conditions does trial NCT02659215 study?

This clinical trial studies the following conditions: Defect of Articular Cartilage. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02659215?

The interventions under investigation include: Microfracture (PROCEDURE), Hyalofast (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02659215?

This trial is sponsored by Anika Therapeutics, which has 30 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02659215 being conducted?

This trial has 20 study locations across Arizona, California, Connecticut, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial