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Wound Dressing
Marine polysaccharide dressing for Venous Leg Ulcer
N/A
Waitlist Available
Research Sponsored by Medline Industries
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Subject is able and willing to comply with requirements of this trial protocol
Voluntarily signed informed consent before any trial related procedures are performed
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to 56 days
Awards & highlights
Study Summary
This trial will compare two types of dressings for venous leg ulcers, to see which is more effective in terms of wound size and surrounding skin condition.
Eligible Conditions
- Venous Leg Ulcer
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline to 56 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to 56 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Wound size changes
Secondary outcome measures
Change in surface area of the dressing
Evaluation of peri-ulcer skin assessment scale
Evaluation of subject pain perception during dressing changes using a numerical pain scale
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Marine polysaccharide dressingExperimental Treatment1 Intervention
Group II: Carboxymethylcellulose dressingActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Marine polysaccharide dressing
2019
N/A
~70
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Who is running the clinical trial?
Medline IndustriesLead Sponsor
45 Previous Clinical Trials
22,980 Total Patients Enrolled
Frequently Asked Questions
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