Neonatal Outcome by Reason for Delivery
Public ClinicalTrials.gov record NCT01818518. 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.
Official title
Neonatal Outcome by Reason for Delivery - A Prospective, Observational Study
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
To determine the rate of Composite Neonatal Morbidity for very preterm babies delivered secondary to preterm labor (PTL) vs. prelabor rupture of membranes (PROM). Composite neonatal morbidity is defined as ≥ 1 of the following: Respiratory Distress Syndrome (RDS) (oxygen requirement, clinical diagnosis, and consistent chest radiograph), bronchopulmonary dysplasia (BPD) (requirement for oxygen support at 28 days of life), severe intraventricular hemorrhage (IVH) (grades III or IV), periventricular leukomalacia (PVL), blood culture-proven sepsis, necrotizing enterocolitis (NEC), or perinatal death (stillbirth or death before neonatal hospital discharge.
Study identification
- NCT ID
- NCT01818518
- Recruitment status
- Completed
- Study type
- Observational
- Phase
- Not listed
- Enrollment
- 995 participants
Conditions and interventions
Conditions
Interventions
Not listed
Eligibility (public fields only)
- Age range
- 18 Years to 65 Years
- Sex
- Female
- 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 30, 2013
- Primary completion
- May 2, 2016
- Completion
- Jul 24, 2016
- Last update posted
- Jun 17, 2019
2013 – 2016
United States locations
- U.S. sites
- 10
- U.S. states
- 6
- U.S. cities
- 10
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Banner Desert Medical Center | Mesa | Arizona | 85210 | — |
| Banner Good Samaritan Medical Center | Phoenix | Arizona | 85006 | — |
| Scottsdale Healthcare-Shea Medical Center | Scottsdale | Arizona | 85260 | — |
| Saddleback Memorial Medical Center | Laguna Hills | California | 92653 | — |
| Good Samaritan Hospital | San Jose | California | 95008 | — |
| Presbyterian/St Luke's Hospital | Denver | Colorado | 80218 | — |
| Saint Luke's Hospital, Kansas City | Kansas City | Missouri | 64111 | — |
| Mercy Hospital of St. Louis | St Louis | Missouri | 63141 | — |
| Harris Methodist Hospital - Fort Worth | Fort Worth | Texas | 76104 | — |
| Swedish Medical Center | Seattle | Washington | 98122-4307 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01818518, 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 Jun 17, 2019 · Synced Sep 4, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01818518 live on ClinicalTrials.gov.