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NCT07632001 · ClinicalTrials.gov registry record · NA
Miro3D Wound Matrix for Treatment of Diabetic Foot Ulcers
A NA study, sponsored by Reprise Biomedical.
- Recruiting
- Registry status
- NA
- Development phase
- 180
- Enrollment target
NCT07632001 is a NA study that is actively recruiting participants, run by Reprise Biomedical. The registered enrollment target is 180 participants.
The verdict
NCT07632001, a NA study, is actively recruiting participants, sponsored by Reprise Biomedical.
- RECRUITING
- Registry status
- NA
- Development phase
- 180 participants
- Enrollment target
Study Summary
This study is designed to evaluate whether the Miro3D Wound Matrix, when used in addition to standard of care, improves healing outcomes in patients with chronic diabetic foot ulcers. Diabetic foot ulcers are a common and serious complication of diabetes and may be difficult to heal despite appropriate treatment. Standard of care typically includes regular wound cleaning, debridement (removal of dead tissue), offloading (reducing pressure on the wound), and moisture-balancing dressings. However, some wounds fail to heal with standard treatment alone. Miro3D Wound Matrix is a three-dimensional, acellular scaffold derived from porcine tissue that is intended to support wound healing. This study will compare outcomes in patients treated with Miro3D plus standard of care versus standard of care alone. Approximately 180 adult subjects with non-healing diabetic foot ulcers will be enrolled at multiple clinical sites in the United States. After a two-week screening period, eligible participants will be randomly assigned to receive either Miro3D in addition to standard of care or standard of care alone. Subjects will be followed for up to 12 weeks with weekly clinic visits. The primary objective of the study is to determine whether treatment with Miro3D increases the rate of complete wound closure and improves reduction in wound size compared to standard of care alone. Safety will also be evaluated by monitoring adverse events throughout the study.
Interventions
- OTHER Standard of Care
- DEVICE Miro3D Wound Matrix
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 180 participants |
| Start Date | 2026-06 |
| Est. Completion | 2027-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07632001
The ClinicalTrials.gov registry entry for NCT07632001 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 180 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Reprise Biomedical, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Standard of Care is the first listed.
NCT07632001 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT07632001 about?
NCT07632001 is a clinical study titled "Miro3D Wound Matrix for Treatment of Diabetic Foot Ulcers". This study is designed to evaluate whether the Miro3D Wound Matrix, when used in addition to standard of care, improves healing outcomes in patients with chronic diabetic foot ulcers. Diabetic foot ulcers are a common and serious complication of diabetes and may be difficult to heal despite appropr...
What is the current status of trial NCT07632001?
This trial is currently recruiting. It is a NA study. The enrollment target is 180 participants. The study started on 2026-06. Estimated completion is 2027-05.
What interventions are being tested in trial NCT07632001?
The interventions under investigation include: Standard of Care (OTHER), Miro3D Wound Matrix (DEVICE).
Who is sponsoring clinical trial NCT07632001?
This trial is sponsored by Reprise Biomedical, which has 3 total clinical trials registered on ClinicalTrials.gov.
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