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Antimicrobial Agent
Silver Alginate for Central Line-Associated Bloodstream Infection
N/A
Waitlist Available
Led By Asif Khattak, MD
Research Sponsored by Baylor Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights
Study Summary
The purpose of this study is to determine whether silver alginate (Algidex) patch is effective in the prevention of central line infections in very low birth weight infants.
Eligible Conditions
- Central Line-Associated Bloodstream Infection
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
The primary objective of this trial is to assess the efficacy of silver alginate dressing in reducing central line infections in VLBW infants
Secondary outcome measures
Medical dressing
Trial Design
1Treatment groups
Active Control
Group I: No interventionActive Control1 Intervention
Find a Location
Who is running the clinical trial?
Baylor Research InstituteLead Sponsor
200 Previous Clinical Trials
202,926 Total Patients Enrolled
DeRoyal Industries, Inc.Industry Sponsor
5 Previous Clinical Trials
449 Total Patients Enrolled
Asif Khattak, MDPrincipal InvestigatorBaylor Health Care System
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