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Prophylactic DR-CPAP on Late Preterm Infants Born by C-section: an RCT
NCT05204719 · View on ClinicalTrials.gov ↗
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 |
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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. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 306 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05204719 reports 5 study locations spanning 5 distinct geographic areas — top geographies include Indiana, Missouri, Oklahoma. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05204719?
The interventions under investigation include: Prophylactic Delivery Room Continuous Positive Airway Pressure (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05204719?
This trial is sponsored by University of Oklahoma, which has 306 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
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.
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