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Performance of WOUNDCHEK Bacterial Status
NCT06501105 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this clinical study is to evaluate the performance of WOUNDCHEK™ Bacterial Status (WCBS) when the test result is used to inform treatment decisions.
Conditions Studied
Interventions
- DEVICE WOUNDCHEK Bacterial Status
Study Locations (1)
New York
- Northwell Health Comprehensive Wound Healing & Hyperbaric Center — Lake Success
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2024-06-18 |
| Est. Completion | 2024-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06501105
The ClinicalTrials.gov registry entry for NCT06501105 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 75 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Woundchek Laboratories, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Wound Heal appearing as the primary indexed condition, and to 1 intervention — of which WOUNDCHEK Bacterial Status 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: NCT06501105 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. 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 NCT06501105 about?
NCT06501105 is a clinical study titled "Performance of WOUNDCHEK Bacterial Status". The purpose of this clinical study is to evaluate the performance of WOUNDCHEK™ Bacterial Status (WCBS) when the test result is used to inform treatment decisions.
What is the current status of trial NCT06501105?
This trial is currently recruiting. The enrollment target is 75 participants. The study started on 2024-06-18. Estimated completion is 2024-12.
What conditions does trial NCT06501105 study?
This clinical trial studies the following conditions: Wound Heal. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06501105?
The interventions under investigation include: WOUNDCHEK Bacterial Status (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06501105?
This trial is sponsored by Woundchek Laboratories, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06501105 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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