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NCT03633877 · ClinicalTrials.gov registry record · NA
Durapore vs. Hy-Tape to Secure The Endotracheal Tube
A NA study, sponsored by Tufts Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 112
- Enrollment target
NCT03633877 is a NA study that has completed, run by Tufts Medical Center. The registered enrollment target is 112 participants.
The verdict
NCT03633877, a NA study, has completed, sponsored by Tufts Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 112 participants
- Enrollment target
Study Summary
While adhesive tape is commonly used to secure endotracheal tubes (ETT) during general anesthesia, its use is also associated with facial skin injuries. Although a variety of adhesive tapes are used in clinical practice, few studies have investigated the likelihood of adhesives in producing injury. The purpose of this randomized, controlled, non-inferiority study was to compare the proportion of facial skin injury with Durapore™ vs. Hy-Tape®.
Interventions
- DEVICE DuraporeTM and Hy-Tape®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 112 participants |
| Start Date | 2018-09-17 |
| Est. Completion | 2019-10-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03633877
The ClinicalTrials.gov registry entry for NCT03633877 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 112 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tufts Medical Center, which has 169 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which DuraporeTM and Hy-Tape® is the first listed.
NCT03633877 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03633877 about?
NCT03633877 is a clinical study titled "Durapore vs. Hy-Tape to Secure The Endotracheal Tube". While adhesive tape is commonly used to secure endotracheal tubes (ETT) during general anesthesia, its use is also associated with facial skin injuries. Although a variety of adhesive tapes are used in clinical practice, few studies have investigated the likelihood of adhesives in producing injury. ...
What is the current status of trial NCT03633877?
This trial is currently completed. It is a NA study. The enrollment target is 112 participants. The study started on 2018-09-17. Estimated completion is 2019-10-11.
What interventions are being tested in trial NCT03633877?
The interventions under investigation include: DuraporeTM and Hy-Tape® (DEVICE).
Who is sponsoring clinical trial NCT03633877?
This trial is sponsored by Tufts Medical Center, which has 169 total clinical trials registered on ClinicalTrials.gov.
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