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Recover L-PRP in Lateral Epicondylitis (REGP-11-00)

NCT02588040 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 18

Last updated 2018-01-10

No results posted yet for this study

Summary

The objective of the study is to further characterize the performance of L-PRP prepared using the Biomet Recover Kit in the treatment of chronic LE. The study will explore the potential impact of patient demographics and baseline characteristics on treatment outcome. Furthermore it will track and document treatment effects, time course, and untoward effects following treatment of chronic LE with L-PRP from the Recover device. In addition, the utilization of healthcare resources and associated costs will be investigated in treated patients.

Conditions

  • Lateral Epicondylitis

Interventions

BIOLOGICAL

Leukocyte- and Platelet-Rich Plasma (L-PRP)

The Recover L-PRP Mini Platelet Separation Kit aids in the separation of the patient's own blood components by density through the use of a Biomet Biologics centrifuge.

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Adam Watts, MD · Wrightington Hospital, Wigan, United Kingdom

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2017-09-30
Completion
2017-09-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02588040 on ClinicalTrials.gov