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Dressing
PermeaDerm® for Thermal Burns
N/A
Recruiting
Led By David Greenhalgh, M.D.
Research Sponsored by Stedical Scientific, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 and 12 months
Awards & highlights
Study Summary
This trial will test the effectiveness of two different types of dressings for treating partial thickness burns.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 and 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 and 12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Reepithelialization
Secondary outcome measures
Adverse Events
Alternate therapy
Dressing Changes Required
+4 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: PermeaDerm®Experimental Treatment1 Intervention
N=34 Participants will receive application of PermeaDerm® as outlined in Directions for Use
Group II: Mepilex Ag®Active Control1 Intervention
Participants will receive application of Mepilex Ag® as outlined in Directions for Use.
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Who is running the clinical trial?
Stedical Scientific, Inc.Lead Sponsor
David Greenhalgh, M.D.Principal InvestigatorUniversity of California, Davis
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have experienced burns from electricity, chemicals, or extreme cold.You have burns covering 20% or more of your total body surface area.Your medical history or current medication use could affect your ability to heal properly from wounds. This includes conditions like diabetes, smoking, drug abuse, and autoimmune disease.Your wound(s) must not be too severe or deep for the study treatment to be used.
Research Study Groups:
This trial has the following groups:- Group 1: PermeaDerm®
- Group 2: Mepilex Ag®
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: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is there any availability for participants in this research experiment?
"This clinical trial, which was created on February 2nd 2022 and edited recently on June 21st 2022, is actively recruiting patients."
Answered by AI
What is the current enrollment of this research project?
"Affirmative. Clinicaltrials.gov features the study's posting, which was first introduced on February 2nd 2022 and modified most recently on June 21st 2022. This clinical trial is actively seeking 68 participants from a single medical site."
Answered by AI
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