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A Prospective, Single-arm, Trial to Determine Contamination Rates When Using an Antibacterial Incise Drape During Orthopedic Surgery
NCT07356323 · View on ClinicalTrials.gov ↗
Study Summary
The goal of this clinical study is to generate data on the intended use of a chlorhexidine gluconate (CHG)-impregnated antimicrobial incise drape. The study includes subjects undergoing primary hip or knee arthroplasty procedures. The study evaluates the intraoperative performance and safety of the incise drape during surgery, including assessment of contamination and operative characteristics. Participants will have a CHG-impregnated antimicrobial incise drape applied during their surgical procedure. During surgery, samples will be collected from the operative site to assess potential bacterial contamination.
Conditions Studied
Interventions
- DEVICE 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (2% w/w CHG)
Study Locations (2)
Indiana
- Indiana University Health (IU Health) — Fishers
Utah
- University of Utah Health - Department of Orthopedics — Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 179 participants |
| Start Date | 2026-02-19 |
| Est. Completion | 2026-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07356323
The ClinicalTrials.gov registry entry for NCT07356323 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 179 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Solventum US, which has 13 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Arthroplasty Replacement, Knee appearing as the primary indexed condition, and to 1 intervention — of which 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (2% w/w CHG) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07356323 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Indiana, Utah. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07356323 about?
NCT07356323 is a clinical study titled "A Prospective, Single-arm, Trial to Determine Contamination Rates When Using an Antibacterial Incise Drape During Orthopedic Surgery". The goal of this clinical study is to generate data on the intended use of a chlorhexidine gluconate (CHG)-impregnated antimicrobial incise drape. The study includes subjects undergoing primary hip or knee arthroplasty procedures. The study evaluates the intraoperative performance and safety of the...
What is the current status of trial NCT07356323?
This trial is currently recruiting. It is a NA study. The enrollment target is 179 participants. The study started on 2026-02-19. Estimated completion is 2026-05.
What conditions does trial NCT07356323 study?
This clinical trial studies the following conditions: Arthroplasty Replacement, Knee, Arthroplasty Total Hip Replacement. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07356323?
The interventions under investigation include: 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (2% w/w CHG) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07356323?
This trial is sponsored by Solventum US, which has 13 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07356323 being conducted?
This trial has 2 study locations across Indiana, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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