Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT05204719 · ClinicalTrials.gov registry record · NA
Prophylactic DR-CPAP on Late Preterm Infants Born by C-section: an RCT
A NA study of Premature Birth, sponsored by University of Oklahoma.
- Active
- Registry status
- NA
- Development phase
- 120
- Enrollment target
- 5
- Study locations
NCT05204719 is a NA study of Premature Birth that is active but no longer recruiting, run by University of Oklahoma. The registered enrollment target is 120 participants, below the 391-participant average among 38 other Premature Birth trials with a reported enrollment target (69% lower). The trial reports 5 study locations across 5 states.
The verdict
NCT05204719, a NA study of Premature Birth, is active but no longer recruiting, sponsored by University of Oklahoma.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 120 participants
- Enrollment target
- 5
- Study locations
Study Summary
A Pragmatic Randomized Controlled Pilot Trial to Evaluate the Impact of Early Prophylactic Continuous Positive Airway Pressure with or without Supplemental Oxygen in Spontaneously Breathing Late Preterm Newborn Infants Born by Cesarean Delivery, Compared to No Early Prophylactic Continuous Positive Airway Pressure with or without Supplemental Oxygen, on the Need for Further Respiratory Support Leading to NICU Admissions.
Conditions Studied
Interventions
- PROCEDURE Prophylactic Delivery Room Continuous Positive Airway Pressure
Study Locations (5)
Indiana
- Indiana University - Indianapolis
Missouri
- Saint Louis University - St Louis
Oklahoma
- The University of Oklahoma Health Campus - Oklahoma City
Alberta
- University of Alberta - Edmonton
Santiago Metropolitan
- Pontificia Universidad Católica de Chile - Santiago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2023-08-04 |
| Est. Completion | 2025-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05204719
The ClinicalTrials.gov registry entry for NCT05204719 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 391-participant average among 38 other Premature Birth trials with a reported enrollment target (69% lower). The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Premature Birth appearing as the primary indexed condition, and to 1 intervention - of which Prophylactic Delivery Room Continuous Positive Airway Pressure is the first listed.
NCT05204719 reports 5 study locations spanning 5 distinct geographic areas - top geographies include Indiana, Missouri, Oklahoma.
Frequently Asked Questions
What is clinical trial NCT05204719 about?
NCT05204719 is a clinical study titled "Prophylactic DR-CPAP on Late Preterm Infants Born by C-section: an RCT". A Pragmatic Randomized Controlled Pilot Trial to Evaluate the Impact of Early Prophylactic Continuous Positive Airway Pressure with or without Supplemental Oxygen in Spontaneously Breathing Late Preterm Newborn Infants Born by Cesarean Delivery, Compared to No Early Prophylactic Continuous Positive ...
What is the current status of trial NCT05204719?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2023-08-04. Estimated completion is 2025-12.
What conditions does trial NCT05204719 study?
This clinical trial studies the following conditions: Premature Birth.
What interventions are being tested in trial NCT05204719?
The interventions under investigation include: Prophylactic Delivery Room Continuous Positive Airway Pressure (PROCEDURE).
Who is sponsoring clinical trial NCT05204719?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05204719 being conducted?
This trial has 5 study locations across Indiana, Missouri, Oklahoma, Alberta, Santiago Metropolitan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Premature Birth
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
A Randomized Controlled Trial of Impact of Wearable, Wireless Breast Pumps on Frequency and Efficacy of Milk Expression in Mothers of Premature Infants
RECRUITING · NA
-
Optimizing Family Counseling for Anticipated Extremely Preterm Delivery
RECRUITING · NA
-
The Periviable GOALS Decision Support Tool
RECRUITING · NA
-
Postpartum Care in the NICU (PeliCaN) Transitions
RECRUITING · NA
-
Development of a Therapeutic Device to Improve Speech Sound Differentiation in Preterm Infants
RECRUITING · NA
-
Healing Tiny Minds: Rural Recovery Through Virtual and Lived Experience Care
RECRUITING · NA
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.