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Tornier Blueprint Planning Software in Patients Receiving Reverse Shoulder Arthroplasty

NCT04474665 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2020-07-17

No results posted yet for this study

Summary

Compare sizing determined in pre-operative planning of reverse shoulder arthroplasty to operative implant size selected.

Conditions

  • Reverse Shoulder Replacement

Interventions

DEVICE

Reverse shoulder arthroplasty utilizing Blueprint Software

Reverse shoulder arthroplasty utilizing Blueprint Software

Sponsors & Collaborators

  • Stryker Trauma and Extremities

    collaborator INDUSTRY

  • Spine Institute of Louisiana Foundation

    lead INDUSTRY

Principal Investigators

  • David Googe, MD · Orthopedics Specialists of Louisiana

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-03-16
Primary Completion
2021-06-01
Completion
2021-06-01
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 NCT04474665 on ClinicalTrials.gov