CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 50 enrolled
Drug / intervention
End tidal CO2 monitordevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01381068
NCT01381068N/ACompleted
CompareCT.gov

Quantitative End Tidal CO2 Monitoring in the Delivery Room: Can we Prevent Hypo/Hypercapnia Upon Admission to the NICU?

Neil Finer·interventional·Posted Jun 27, 2011·Updated Dec 17, 2019

In Brief

A clinical study evaluating End tidal CO2 monitor for Delivery Room Resuscitation. Completed, enrolled 50 participants across 1 site.

Detailed Summary

This is a trial evaluating the use of an end tidal CO2 monitor during ventilation in the delivery room. The use of the monitor is compared with clinical assessment of ventilation. The hypothesis is that using the monitor would results in a decrease in the incidence of hypo- or hypercapnia on admission to the NICU.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDelivery Room Resuscitation
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedJun 27, 2011
Enrollment StartOct 1, 2009
Primary CompletionMay 1, 2011
Study CompletionSep 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 15.0 years ago

Interventions

End tidal CO2 monitordevice

The sensor is placed in the respiratory circuit in both arms of the trial but the display is visible to the resuscitation team in the monitored arm and is covered in the control arm. The end tidal CO2 data is collected in both arms.