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Antimicrobial Wound Dressing
Intervention Period for Foot Ulcer
N/A
Waitlist Available
Research Sponsored by Chester Ho, MD
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 through study completion over four months
Awards & highlights
Study Summary
This trial evaluates the effectiveness of a new wound dressing, NanoSALV, to improve chronic wound care, cost-savings, patient satisfaction, and healing time. Interviews and observations are used to assess usability.
Eligible Conditions
- Diabetic Foot Ulcers
- Pressure Ulcer
- Leg Ulcer
- Venous Leg Ulcer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion over four months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion over four months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Process Improvement
Quality Improvement
Soft Cost Savings
+2 moreSecondary outcome measures
Adverse events
Patient preference
Patient satisfaction - comfort
+4 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention PeriodExperimental Treatment1 Intervention
Patients receive the intervention, NanoSALV wound dressing, in the consecutive four weeks following the control period
Group II: Control PeriodActive Control1 Intervention
Patients receive the current standard of care for their chronic wound in the first four weeks of enrollment
Standard of care (SOC) involves:
Offloading of pressure as needed
High compression bandaging, as needed
Debridement, as needed
Nutrition management, as needed
SOC dressings, such as silver/iodine dressings, antibiotic ointment
Management of infection
Management of pain during debridement, as needed
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
NanoSALV Catalytic
2022
N/A
~50
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Who is running the clinical trial?
Chester Ho, MDLead Sponsor
Alberta Health servicesOTHER
158 Previous Clinical Trials
649,625 Total Patients Enrolled
NanoTess Inc.UNKNOWN
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