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NCT06598241 · ClinicalTrials.gov registry record
Mirragen Diabetic Foot Ulcer Study
A clinical trial of Diabetic Foot Ulcer and Osteomyelitis Chronic, sponsored by The University of Texas Health Science Center at San Antonio.
- Recruiting
- Registry status
- 20
- Enrollment target
- 1
- Study location
NCT06598241 is a study of Diabetic Foot Ulcer and Osteomyelitis Chronic that is actively recruiting participants, run by The University of Texas Health Science Center at San Antonio. The registered enrollment target is 20 participants, below the 255-participant average among 67 other Diabetic Foot Ulcer trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06598241, a study of Diabetic Foot Ulcer and Osteomyelitis Chronic, is actively recruiting participants, sponsored by The University of Texas Health Science Center at San Antonio.
- RECRUITING
- Registry status
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
This study is being done to collect data from treatment of patients who have diabetes with non-healing foot wounds and are being treated with a resorbable and biocompatible borate-based bioactive glass fiber matrix. A borate-based bioactive glass fiber matrix is used to cover the ulcer for wound management. The primary objective of this study is to evaluate the safety and efficacy of the borate-based bioactive glass fiber matrix in the treatment of diabetic foot ulcers in a real-world setting. The secondary objective is to evaluate the clinical and financial benefits in terms of quality of healing, pain, and treatment cost.
Conditions Studied
Interventions
- DEVICE Borate-base Bioactive Glass Fiber Matrix (BBGFM)
Study Locations (1)
Texas
- UT Health Medical Arts and Research Center - San Antonio
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2024-09-20 |
| Est. Completion | 2026-11 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06598241
The ClinicalTrials.gov registry entry for NCT06598241 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 255-participant average among 67 other Diabetic Foot Ulcer trials with a reported enrollment target (92% lower). The listed sponsor is The University of Texas Health Science Center at San Antonio, which has 378 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Diabetic Foot Ulcer appearing as the primary indexed condition, and to 1 intervention - of which Borate-base Bioactive Glass Fiber Matrix (BBGFM) is the first listed.
NCT06598241 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT06598241 about?
NCT06598241 is a clinical study titled "Mirragen Diabetic Foot Ulcer Study". This study is being done to collect data from treatment of patients who have diabetes with non-healing foot wounds and are being treated with a resorbable and biocompatible borate-based bioactive glass fiber matrix. A borate-based bioactive glass fiber matrix is used to cover the ulcer for wound man...
What is the current status of trial NCT06598241?
This trial is currently recruiting. The enrollment target is 20 participants. The study started on 2024-09-20. Estimated completion is 2026-11.
What conditions does trial NCT06598241 study?
This clinical trial studies the following conditions: Diabetic Foot Ulcer, Osteomyelitis Chronic.
What interventions are being tested in trial NCT06598241?
The interventions under investigation include: Borate-base Bioactive Glass Fiber Matrix (BBGFM) (DEVICE).
Who is sponsoring clinical trial NCT06598241?
This trial is sponsored by The University of Texas Health Science Center at San Antonio, which has 378 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06598241 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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