N/A
N=35
Retention of Nasoenteric Feeding Tubes in Pediatric Patients Using a Nasal Bridle
Feeding Tube Complication
Bottom Line
View on ClinicalTrials.gov: NCT04621734 ↗Enrolled (actual)
35
Serious AEs
0.0%
Results posted
Aug 2023
Primary outcome: Primary: Number of Tube Dislodgements Per 10 Tube Days. — 0.16; 2.11 Dislodgements
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- AMT BridlePro Device (Device); Adhesive Tape (Device)
- Age
- Pediatric, Adult
- Sex
- All
- Sponsor
- The University of Texas Health Science Center at San Antonio
- Primary completion
- Apr 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Tube Dislodgements Per 10 Tube Days. |
0.16; 2.11 | — |
Summary
A study to compare tube dislodgment rates when a nasoenteric feeding tube is secured with adhesive tape vs the AMT BridlePro device.
Eligibility Criteria
Inclusion Criteria
- Need for nasoenteric feeding
- Admitted to University Hospital
- Age 0-18 years
Exclusion Criteria
- Facial trauma
- Nasal airway obstructions
- Thrombocytopenia (<100 K/μL)
- s/p septoplasty
- Patients with vomer bone graft
- Nasoenteric feeding tube placed and secured prior to being screened for study
- Contraindication for the use of the BridlePro
- Does not meet inclusion criteria
Data sourced from ClinicalTrials.gov (NCT04621734). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.