Impact of Glenosphere Size on Range of Motion in Female Patients Undergoing Reverse Shoulder Arthroplasty

Status unconfirmed · Not applicable

Conditions studied: Rotator Cuff Tear Arthropathy, Massive Irreparable Rotator Cuff Tear

In brief

The purpose of this study is to perform a prospective randomized trial among female patients undergoing reverse shoulder arthroplasty (RSA) to determine if a larger glenosphere allows greater range of motion without an impact on complications.

Key facts

Study ID

NCT04093804

Run by

Fondren Orthopedic Group L.L.P.

People needed

120

Starts

2019-10-01

Expected to finish

2024-09-01

Last updated by the study team

2019-09-18

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Female sex
• Diagnosis of rotator cuff tear arthropathy or a massive irreparable rotator cuff tear for which the patient has elected to undergo reverse shoulder arthroplasty
• No history of prior shoulder arthroplasty
• Consent to study participation by signing the informed consent and the Protected Health Information (PHI) form (Attachment B and C)
• Ability to speak, read and write English

You may not qualify if…

• Male sex
• Any impairment that would prevent answering the surveys
• No children or adolescents under the age of 18 years old
• No prisoners, pregnant women, or mentally disabled persons
• No Workers' Compensation cases

Where it is running

• Fondren Orthopedic Group, L.L.P. — Houston, Texas, United States

Full record on ClinicalTrials.gov

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