Your session is about to expire
← Back to Search
Aerosolized Tobramycin or Vancomycin for Ventilator-Associated Pneumonia (AAINTVAP Trial)
Phase 4
Waitlist Available
Led By John K. Bini, MD
Research Sponsored by Wright State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Clinical Pulmonary Infection Score (CPIS) greater than or equal to 6
Intubated greater than or equal to 48 hours
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 9-21 days after initiating antibiotic therapy
Awards & highlights
AAINTVAP Trial Summary
The purpose of this study is to determine if administering inhaled antibiotics directly into the lungs in conjunction with intravenous (IV) antibiotics leads to better outcomes and decreased recurrence of ventilator associated pneumonia (VAP) when compared to IV antibiotics alone.
Eligible Conditions
- Ventilator-Associated Pneumonia
AAINTVAP Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowAAINTVAP Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 9-21 days after initiating antibiotic therapy
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9-21 days after initiating antibiotic therapy
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Persistence of Pneumonia
Recurrence of Pneumonia
Secondary outcome measures
28-day ICU Mortality
Emergence of Resistant Organisms
Intensive Care Unit (ICU) -Free Days in 28 Days
+4 moreAAINTVAP Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Aerosolized Tobramycin or VancomycinExperimental Treatment1 Intervention
Aerosolized tobramycin 300 mg diluted in 5 mL 0.9% normal saline q.12h. Aerosolized vancomycin 125 mg diluted in 5 mL 0.9% normal saline q.8h.
Group II: Aerosolized PlaceboPlacebo Group1 Intervention
Placebo tobramycin 0.5 mL 0.9% normal saline q.12h. Placebo vancomycin 0.5 mL 0.9% normal saline q.8h.
Find a Location
Who is running the clinical trial?
Wright State UniversityLead Sponsor
41 Previous Clinical Trials
54,866 Total Patients Enrolled
Priti Parikh, PhDStudy DirectorWright State University
John K. Bini, MDPrincipal InvestigatorWright State University
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Share this study with friends
Copy Link
Messenger