Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02692573 · ClinicalTrials.gov registry record · NA

Prone or Supine Effect After Caesarean Delivery on Respiratory Outcomes in Full Term Infants

A NA study, sponsored by Montefiore Medical Center.

Completed
Registry status
NA
Development phase
500
Enrollment target

NCT02692573: Completed NA study, sponsored by Montefiore Medical Center.

NCT02692573 is a NA study that has completed, run by Montefiore Medical Center. The registered enrollment target is 500 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (64% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02692573, a NA study, has completed, sponsored by Montefiore Medical Center.

COMPLETED
Registry status
NA
Development phase
500 participants
Enrollment target

Study Summary

Investigators will compare 500 full term babies delivered by SCD randomized into two groups, prone or supine position. Investigators will use a Panda warmer with built in Nellcor pulse oximeter. Each infant will have heart rate (HR), oxygen saturation via pulse oximetry, respiratory rate and respiratory effort documented every 1 minute for the first 5 minutes of life; beyond the initial 5minutes of life, monitoring as well as infant's management will be done as per current Weiler hospital protocols. The intervention group will be placed in prone position for first five minutes immediately after birth, and then changed to supine position. The control group will be placed supine from birth. Investigators will check for the incidence and severity of RD, supplemental oxygen need and duration, positive pressure ventilation (PPV) need and duration or other use of respiratory support (intubation). Additionally, investigators will record the number of infants requiring admission to the NICU in each group, days of ventilatory support as well as the length of hospitalization.

Primary Outcome

any administration of positive pressure ventilation and /or oxygen

Interventions

  • OTHER positioning

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2015-12
Est. Completion 2018-12-18
Phase NA
Montefiore Medical Center

345 total trials

What the finished NCT02692573 record still lists

NCT02692573 is an interventional study that assigns participants to a tested intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (64% lower).

The record links to 0 conditions, and to 1 intervention - of which positioning is the first listed.

NCT02692573 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02692573 about?

NCT02692573 is a clinical study titled "Prone or Supine Effect After Caesarean Delivery on Respiratory Outcomes in Full Term Infants". Investigators will compare 500 full term babies delivered by SCD randomized into two groups, prone or supine position. Investigators will use a Panda warmer with built in Nellcor pulse oximeter. Each infant will have heart rate (HR), oxygen saturation via pulse oximetry, respiratory rate and respira...

What is the current status of trial NCT02692573?

This trial is currently completed. It is a NA study. The enrollment target is 500 participants. The study started on 2015-12. Estimated completion is 2018-12-18.

What interventions are being tested in trial NCT02692573?

The interventions under investigation include: positioning (OTHER).

Who is sponsoring clinical trial NCT02692573?

This trial is sponsored by Montefiore Medical Center, which has 345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02692573's enrollment target sits among peer trials

500 193rd of 2000 higher than 1,788 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00001230 · 500 participants

    Host Response to Infection and Treatment in Filarial Diseases

  • NCT00001529 · 500 participants

    Improved Methods of Cell Selection for Bone Marrow Transplant Alternatives

  • NCT00697411 · 500 participants

    Study of Selected X-Linked Disorders: Aicardi Syndrome

  • NCT00903110 · 500 participants

    Global Patient Registry to Monitor Long-term Safety and Effectiveness of Increlex® in Children and Adolescents With Severe Primary Insulin-like Growth Factor-1 Deficiency (SPIGFD).

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02692573, the US trial registry maintained by the National Library of Medicine. NCT02692573 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.