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Outcomes Following Delta Xtend Reverse Shoulder System

NCT ID: NCT02014350

Last Updated: 2013-12-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Study Classification

OBSERVATIONAL

Brief Summary

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To collect medium to long-term survivorship implant outcomes on the DePuy Delta Xtend Reverse Shoulder Stystem.

Detailed Description

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Conditions

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Reverse Total Shoulder Arthroplasty

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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DePuy Delta Xtend RTSA

DePuy Delta Xtend Reverse TSA

Intervention Type DEVICE

Interventions

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DePuy Delta Xtend Reverse TSA

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

Patients whom were implanted with the DePuy Delta Xtend Reverse Total Shoulder System in the time frame indicated. Patients must be willing to sign the consent form and complete all follow-up visits.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Rothman Institute Orthopaedics

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Rothman Institute

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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RI2013

Identifier Type: -

Identifier Source: org_study_id