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Clinical Study Evaluating Wound Closure With Endoform™ and Symphony™
NCT06035523 · View on ClinicalTrials.gov ↗
Study Summary
Study will evaluate the performance and safety of Endoform™ Natural and Endoform™ Antimicrobial in conjunction with Symphony™ in the treatment of chronic non-healing diabetic foot ulcers after 12 weeks of treatment.
Conditions Studied
Interventions
- DEVICE Endoform™ Antibacterial
- DEVICE Endoform™ Natural
- DEVICE Symphony™
Study Locations (4)
Florida
- South Florida Lower Extremity Center — Hollywood
- Advanced Pharma Cr, LLC — Miami
Virginia
- Foot and Ankle Specialists of the Mid-Atlantic — Salem
Washington
- Madigan Army Medical Center — Tacoma
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2021-12-29 |
| Est. Completion | 2025-08-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06035523
The ClinicalTrials.gov registry entry for NCT06035523 describes a study currently listed as completed. 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 44 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Aroa Biosurgery Limited, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Diabetic Foot appearing as the primary indexed condition, and to 3 interventions — of which Endoform™ Antibacterial 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: NCT06035523 reports 4 study locations spanning 3 distinct geographic areas — top geographies include Florida, Virginia, Washington. 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 NCT06035523 about?
NCT06035523 is a clinical study titled "Clinical Study Evaluating Wound Closure With Endoform™ and Symphony™". Study will evaluate the performance and safety of Endoform™ Natural and Endoform™ Antimicrobial in conjunction with Symphony™ in the treatment of chronic non-healing diabetic foot ulcers after 12 weeks of treatment.
What is the current status of trial NCT06035523?
This trial is currently completed. It is a NA study. The enrollment target is 44 participants. The study started on 2021-12-29. Estimated completion is 2025-08-30.
What conditions does trial NCT06035523 study?
This clinical trial studies the following conditions: Diabetic Foot, Foot Ulcer, Wound Healing, Chronic Foot Ulcer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06035523?
The interventions under investigation include: Endoform™ Antibacterial (DEVICE), Endoform™ Natural (DEVICE), Symphony™ (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06035523?
This trial is sponsored by Aroa Biosurgery Limited, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06035523 being conducted?
This trial has 4 study locations across Florida, Virginia, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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