Reduction of Bacterial Seeding in Total Shoulder Arthroplasty

Recruiting N/A Interventional Study
Joint Arthroplasty Shoulder Cutibacterium Acnes Prosthetic Joint Infection
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Male
Study type
Interventional
Purpose
Prevention
Participants needed
60 (estimated)
Sponsor
St. Louis University · Other
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About This Trial

The purpose of this study is to compare the growth of intra-operative tissue cultures of Cutibacterium Acnes after primary shoulder replacement when using a no-prep control group versus Prontosan wound gel applied to the skin layer after the skin incision has been made.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult male 18 years of age or older undergoing elective primary total shoulder arthroplasty, including both anatomic and reverse total shoulder arthroplasty, for indications including massive rotator cuffs, rotator cuff arthropathy, glenohumeral osteoarthritis, and acute fract…
Contacts

Randall Otto, MD

314-617-2970

randy.otto@health.slu.edu

CONTACT

Allison Gruender, RN, MSN

314-617-3406

allison.gruender@health.slu.edu

CONTACT