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NuShield in Surgical Peroneal Tendon Repair

NCT03828916 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2020-01-14

No results posted yet for this study

Summary

The purpose of this study is to evaluate the use of NuShield in subjects requiring surgical tendon repair.

Conditions

  • Tendon Injuries
  • Tendinopathy

Interventions

OTHER

NuShield

SOC surgery with the addition of NuShield

Sponsors & Collaborators

  • Organogenesis

    collaborator INDUSTRY

  • NuTech Medical, Inc

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2019-01-30
Primary Completion
2021-06-30
Completion
2021-06-30

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 NCT03828916 on ClinicalTrials.gov