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NuTech Affinity™ for the Treatment of Chondral Defects

NCT02837484 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2020-01-18

No results posted yet for this study

Summary

This study was designed to evaluate the long term effectiveness of a product used in knee surgery called Affinity™ Membrane.

Conditions

  • Chondral Lesions
  • Cartilage

Interventions

OTHER

NuTech Affinity™ Membrane

NuTech Affinity™ Membrane is an aseptically produced hypothermically stored amniotic membrane patch.

Sponsors & Collaborators

  • Organogenesis

    collaborator INDUSTRY

  • NuTech Medical, Inc

    lead INDUSTRY

Principal Investigators

  • Sam Tabet, MD · New Mexico Orthopaedic Associates

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2020-10-31
Completion
2020-10-31

Countries

  • United States

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 NCT02837484 on ClinicalTrials.gov