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Retention of Nasoenteric Feeding Tubes in Pediatric Patients Using a Nasal Bridle
N/A
Waitlist Available
Led By Veronica Armijo, MD
Research Sponsored by The University of Texas Health Science Center at San Antonio
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up period of hospitalization (no more than 30 days)
Summary
A study to compare tube dislodgment rates when a nasoenteric feeding tube is secured with adhesive tape vs the AMT BridlePro device.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ period of hospitalization (no more than 30 days)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~period of hospitalization (no more than 30 days)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Number of Tube Dislodgements Per 10 Tube Days.
Secondary study objectives
Cost of replacement tubes and follow up radiographs
Number of radiographs for tube replacement
Time of missed nutrition
+1 moreTrial Design
2Treatment groups
Active Control
Placebo Group
Group I: Nasal bridle to secure feeding tubeActive Control1 Intervention
The nasal bridle will be used to secure the nasoenteric feeding tube.
Group II: Adhesive Tape use to secure feeding tubePlacebo Group1 Intervention
Adhesive tape will be used as standard of care to secure the nasoenteric feeding tube.
Find a Location
Who is running the clinical trial?
The University of Texas Health Science Center at San AntonioLead Sponsor
477 Previous Clinical Trials
92,935 Total Patients Enrolled
Veronica Armijo, MDPrincipal InvestigatorUniversity of Texas Health at San Antonio