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Collagen Dressing
Fibrillar Collagen Powder Dressing for Wound
N/A
Waitlist Available
Led By Emmy Oji, DPM
Research Sponsored by Medline Industries
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to 84 days
Awards & highlights
No Placebo-Only Group
Summary
Patients who meet the inclusion criteria will be provided with fibrillar collagen powder dressing. The powder dressing will be used in accordance with its label. After cleansing the wound by the clinical site staff, the powder is placed directly on the wound, and then the wound will be covered with an appropriate moisture retentive secondary dressing. Patients will visit the clinic twice a week to have the powder re-applied. Wound evaluations will take place once a week at the outpatient clinic, with the intervention lasting up to twelve weeks. Concurrent standard of care, such as compression for venous ulcers, will be provided.
Eligible Conditions
- Wound
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline to 84 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to 84 days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Secondary study objectives
Change in Bates-Jensen Wound Assessment Tool
Change in reported pain level
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Fibrillar Collagen Powder DressingExperimental Treatment1 Intervention
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Who is running the clinical trial?
Medline IndustriesLead Sponsor
45 Previous Clinical Trials
23,022 Total Patients Enrolled
Emmy Oji, DPMPrincipal InvestigatorValley Foot and Ankle Specialty Providers
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