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Wound Dressing
Transforming Powder Dressing vs Standard Care for Foot Ulcer
N/A
Recruiting
Led By Lawrence Lavery, DPM, MPH
Research Sponsored by ULURU Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Wound drainage is minimal or moderate
Able and willing to provide consent
Timeline
Screening 3 days
Treatment Varies
Follow Up 3 days
Awards & highlights
No Placebo-Only Group
Summary
This trial compares a special healing powder to regular wound dressings for diabetic patients with foot ulcers. The powder aims to help wounds heal faster by keeping them clean and supporting skin recovery.
Who is the study for?
This trial is for adults aged 18-89 with diabetes and a diabetic foot ulcer that's lasted at least 30 days. They should have controlled blood sugar (Hemoglobin A1C <12%) and be able to attend weekly appointments. People with severe illnesses, high BMI (>45), recent steroid use, or heavy wound drainage cannot participate.
What is being tested?
The study compares a new Transforming Powder Dressing against standard care dressings in healing diabetic foot ulcers. It's a Phase IV trial where participants are randomly chosen to receive one of the treatments and monitored over time.
What are the potential side effects?
While specific side effects aren't listed, typical risks may include skin irritation, allergic reactions to dressing materials, or infection due to improper wound management.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 days1 visit
Treatment ~ Varies
Follow Up ~ 3 days1 visit
Screening ~ 3 days
Treatment ~ Varies
Follow Up ~3 days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Incidence of wound closure
Secondary study objectives
Adverse Events
Clinician Acceptability
Quality of Life while living with a wound
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Active Control
Group I: Standard of Care DressingActive Control1 Intervention
Half of the subjects will be randomized to receive standard of care wound dressings to treat their diabetic foot ulcers. Wounds will be evaluated weekly, debrided if needed, photographed, and measured. A wound dressing will be applied using standard of care wound products, and the wound will be offloaded when necessary (pressure taken off of the wound using a total contact cast or other device). Wound healing progress will be monitored and compared to transforming powder dressings used to treat diabetic foot ulcers. Surveys regarding pain and quality of life will be completed at each study visit.
Group II: Transforming Powder DressingActive Control1 Intervention
Half of the subjects will be randomized to Transforming Powder Dressing to treat their diabetic foot ulcers. Wounds will be evaluated weekly, debrided if needed, photographed, and measured. A wound dressing will be applied using Transforming Powder Dressing and the wound will be offloaded when necessary (pressure taken off of the wound using a total contact cast or other device). Wound healing progress will be monitored and compared to other standard of care dressings used to treat diabetic foot ulcers.Surveys regarding pain and quality of life will be completed at each study visit.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for foot ulcers, such as transforming powder dressings, work by creating a moist environment that promotes wound healing. This moist environment is essential as it facilitates cell migration, collagen formation, and tissue regeneration.
Additionally, these dressings can deliver bioactive compounds directly to the wound site, which can further enhance healing by reducing inflammation, preventing infection, and stimulating tissue repair. For foot ulcer patients, these mechanisms are vital as they can significantly accelerate the healing process, reduce complications, and improve the quality of life.
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Logistics
Other reimbursement is provided
Other forms of reimbursement are provided for this trial.
Who is running the clinical trial?
Military Technology Enterprise Consortium (US)UNKNOWN
ULURU Inc.Lead Sponsor
4 Previous Clinical Trials
403 Total Patients Enrolled
Naval Medical Research CenterFED
33 Previous Clinical Trials
2,696 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Standard of Care Dressing
- Group 2: Transforming Powder Dressing
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: You will receive the treatment for 3 null
- Follow Ups: You may be asked to continue sharing information regarding the trial for 3 Months after you stop receiving the treatment.
Foot Ulcer Patient Testimony for trial: Trial Name: NCT05046158 — N/A
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