Evaluation of Structural and Functional Integrity of the Rotator Cuff After Total Shoulder Arthroplasty
NCT ID: NCT03921944
Last Updated: 2025-07-03
Study Results
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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RECRUITING
NA
30 participants
INTERVENTIONAL
2024-05-02
2026-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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total shoulder replacement surgery
Subjects will be assessed for the outcome measures at one year and two year timepoints post total shoulder replacement surgery
CT scan of the shoulders
studies of both operative and nonoperative shoulders
Interventions
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CT scan of the shoulders
studies of both operative and nonoperative shoulders
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* primary diagnosis of osteoarthritis of the shoulder
* total shoulder replacement performed by Dr. Armstrong
* administered a local anesthetic mixture and not regional anesthesia
* all genders
* Fluent in written and spoken English
* Patients capable of giving informed consent
Exclusion Criteria
* Inability to provide informed consent
* History of recent trauma to the shoulder
* Atypical shoulder pain
* Other suspected shoulder pathology (i.e. tumor, infection)
* Pregnancy
* Bilateral total shoulder arthroplasty
45 Years
ALL
No
Sponsors
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Milton S. Hershey Medical Center
OTHER
Responsible Party
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April Armstrong
Professor of Surgery, Orthopaedics
Principal Investigators
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April D Armstrong, MD
Role: PRINCIPAL_INVESTIGATOR
Milton S. Hershey Medical Center
Locations
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Penn State Hershey Medical Center
Hershey, Pennsylvania, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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STUDY00008095
Identifier Type: -
Identifier Source: org_study_id
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