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NCT07406893 · ClinicalTrials.gov registry record · NA
Reduction of Bacterial Seeding in Total Shoulder Arthroplasty
A NA study of Prosthetic-joint Infection and Shoulder, sponsored by St. Louis University.
- Recruiting
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT07406893 is a NA study of Prosthetic-joint Infection and Shoulder that is actively recruiting participants, run by St. Louis University. The registered enrollment target is 60 participants, below the 92-participant average among 9 other Prosthetic-joint Infection trials with a reported enrollment target (35% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07406893, a NA study of Prosthetic-joint Infection and Shoulder, is actively recruiting participants, sponsored by St. Louis University.
- RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Conditions Studied
Interventions
- DEVICE Prontosan Wound Gel
Study Locations (1)
Missouri
- Saint Louis University - St Louis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2026-02-23 |
| Est. Completion | 2026-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07406893
The ClinicalTrials.gov registry entry for NCT07406893 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 92-participant average among 9 other Prosthetic-joint Infection trials with a reported enrollment target (35% lower). The listed sponsor is St. Louis University, which has 107 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Prosthetic-joint Infection appearing as the primary indexed condition, and to 1 intervention - of which Prontosan Wound Gel is the first listed.
NCT07406893 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.
Frequently Asked Questions
What is clinical trial NCT07406893 about?
NCT07406893 is a clinical study titled "Reduction of Bacterial Seeding in Total Shoulder Arthroplasty". 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.
What is the current status of trial NCT07406893?
This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2026-02-23. Estimated completion is 2026-12.
What conditions does trial NCT07406893 study?
This clinical trial studies the following conditions: Prosthetic-joint Infection, Shoulder, Cutibacterium Acnes, Joint Arthroplasty.
What interventions are being tested in trial NCT07406893?
The interventions under investigation include: Prontosan Wound Gel (DEVICE).
Who is sponsoring clinical trial NCT07406893?
This trial is sponsored by St. Louis University, which has 107 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07406893 being conducted?
This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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