# Feasibility and Impact of Volume Targeted Ventilation in the Delivery Room

> **NCT03938532** · NA · TERMINATED · sponsor: **Baystate Medical Center** · enrollment: 20 (actual)

## Conditions studied

- Prematurity
- BPD - Bronchopulmonary Dysplasia
- Respiratory Distress Syndrome, Newborn

## Interventions

- **DEVICE:** Volume Targeted Ventilation (VTV) using the Philips Respironics NM3 monitor
- **DEVICE:** Tidal Volume Measurement using the Philips Respironics NM3 monitor

## Key facts

- **NCT ID:** NCT03938532
- **Lead sponsor:** Baystate Medical Center
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2019-07-11
- **Primary completion:** 2024-12-31
- **Final completion:** 2024-12-31
- **Target enrollment:** 20 (ACTUAL)
- **Why stopped:** Discontinuation of the study Product by manufacturer
- **Last updated:** 2025-02-05


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03938532

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03938532, "Feasibility and Impact of Volume Targeted Ventilation in the Delivery Room". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT03938532. Licensed CC0.

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