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NCT02799875 · ClinicalTrials.gov registry record · NA
Late Permissive Hypercapnia for Intubated and Ventilated Preterm Infants
A NA study, sponsored by University of Alabama at Birmingham.
- Completed
- Registry status
- NA
- Development phase
- 130
- Enrollment target
NCT02799875 is a NA study that has completed, run by University of Alabama at Birmingham. The registered enrollment target is 130 participants.
The verdict
NCT02799875, a NA study, has completed, sponsored by University of Alabama at Birmingham.
- COMPLETED
- Registry status
- NA
- Development phase
- 130 participants
- Enrollment target
Study Summary
Preterm infants, less than 37 weeks gestation with respiratory distress syndrome, who remain ventilated between 7 and 14 days after birth will be randomized to a ventilator strategy of either a higher level of permissive hypercapnia or of a lower level of permissive hypercapnia to determine if either strategy will increase the number of alive ventilator-free days in the 28 days after randomization.
Interventions
- OTHER Higher permissive hypercapnia
- OTHER Lower Permissive Hypercapnia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 130 participants |
| Start Date | 2015-12 |
| Est. Completion | 2021-04 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02799875
The ClinicalTrials.gov registry entry for NCT02799875 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 130 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Higher permissive hypercapnia is the first listed.
NCT02799875 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02799875 about?
NCT02799875 is a clinical study titled "Late Permissive Hypercapnia for Intubated and Ventilated Preterm Infants". Preterm infants, less than 37 weeks gestation with respiratory distress syndrome, who remain ventilated between 7 and 14 days after birth will be randomized to a ventilator strategy of either a higher level of permissive hypercapnia or of a lower level of permissive hypercapnia to determine if eithe...
What is the current status of trial NCT02799875?
This trial is currently completed. It is a NA study. The enrollment target is 130 participants. The study started on 2015-12. Estimated completion is 2021-04.
What interventions are being tested in trial NCT02799875?
The interventions under investigation include: Higher permissive hypercapnia (OTHER), Lower Permissive Hypercapnia (OTHER).
Who is sponsoring clinical trial NCT02799875?
This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.
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