VentFirst: A Multicenter RCT of Assisted Ventilation During Delayed Cord Clamping for Extremely Preterm Infants
Public ClinicalTrials.gov record NCT02742454. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this study is to determine whether providing ventilatory assistance prior to umbilical cord clamping influences the occurrence of intraventricular hemorrhage (IVH) in extremely preterm (EPT) infants, compared to standard care of providing ventilatory assistance after cord clamping.
Study identification
- NCT ID
- NCT02742454
- Recruitment status
- Not listed
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 570 participants
Conditions and interventions
Conditions
Interventions
- Standard 30-60 Seconds Cord Clamping Procedure
- VentFirst 120 Seconds Cord Clamping Procedure
Procedure
Eligibility (public fields only)
- Age range
- Not listed
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jun 2016 (Type not available)
- Primary completion
- Mar 2023 (Actual)
- Completion
- Dec 2023 (Estimated)
- Last update posted
- Oct 30, 2023
2016 – 2023
United States locations
- U.S. sites
- 10
- U.S. states
- 10
- U.S. cities
- 10
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of Alabama at Birmingham | Birmingham | Alabama | 35233 | — |
| University of California, Davis | Sacramento | California | 95817 | — |
| University of Colorado | Denver | Colorado | 80045-2571 | — |
| University of Indiana | Indianapolis | Indiana | 46202 | — |
| Brigham & Women's Hospital | Boston | Massachusetts | 02115-6110 | — |
| Mayo Clinic | Rochester | Minnesota | 55905-0001 | — |
| St. Louis University | St Louis | Missouri | 63103-2006 | — |
| Columbia University Medical Center | New York | New York | 10032 | — |
| Oregon Health & Science University | Portland | Oregon | 37239-0000 | — |
| University of Virginia | Charlottesville | Virginia | 22904-4195 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT02742454, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Oct 30, 2023 · Synced Oct 23, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT02742454 live on ClinicalTrials.gov.