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Rotator Cuff: Does the Vascularity Matter and the Role for PINPOINT

NCT03001050 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2018-02-26

No results posted yet for this study

Summary

The overall goal of doing this study is to improve long term patient function and outcomes in the healing rates of Rotator Cuffs. The investigators would also like to see if this method can be more cost effective and time efficient for Rotator Cuff evaluation during arthroscopy.

Conditions

  • Rotator Cuff Tear

Interventions

DEVICE

PINPOINT System

To use the camera probe and identify the tendon and footprint vascularity at the time of surgery

Sponsors & Collaborators

  • Nirav Amin, MD

    lead OTHER

Principal Investigators

  • Nirav H Amin, MD · Loma Linda University

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-12-20
Primary Completion
2017-12-20
Completion
2017-12-20
FDA Device
Yes

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 NCT03001050 on ClinicalTrials.gov