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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04699708
Other study ID # 291372
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 15, 2021
Est. completion date June 2022

Study information

Verified date June 2021
Source South Tees Hospitals NHS Foundation Trust
Contact Prakash Loganathan, MD
Phone +447481492632
Email pkannanloganathan@nhs.net
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

CO2 data, serving as a proxy marker for tidal volume, might enable titration of tidal volume/pressure thereby providing optimal ventilation during neonatal resuscitation. Currently there is insufficient data on Co2 levels for preterm babies requiring resuscitation. This study involves monitoring of CO2 during preterm stabilisation.


Description:

Measurement of exhaled CO2 in the delivery room is feasible, but clinical benefits of during neonatal transition have not been studied. Volume ventilation in the Neonatal unit has been shown to improve outcomes such BPD or death. Despite the proven benefits of volume ventilation in the neonatal unit volume guided resuscitation at birth remains an unproven and under-studied technique. CO2 data, serving as a proxy marker for tidal volume, might enable titration of tidal volume/pressure thereby providing optimal ventilation during neonatal resuscitation. Currently there is insufficient data on Co2 levels for preterm babies requiring resuscitation. This data would help in finding out optimal resuscitation strategies (Pressures/volume, frequency of breaths) rather than providing the same for all infants throughout the process of resuscitation and would help us in better interpretation Co2 levels in the future resuscitation. Investigators aim to study the impact of various clinical (Gestation, Birth weight, need for intubation/bag-mask ventilation) and resuscitative factors (use of inflation pressures, ventilation pressures, frequency of breaths, face mask ventilation, intubation) on CO2 during preterm stabilisation.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date June 2022
Est. primary completion date March 2022
Accepts healthy volunteers No
Gender All
Age group 23 Weeks to 32 Weeks
Eligibility Inclusion Criteria: 1. All preterm infants = 32 weeks born at the study centres. 2. Needing resuscitative measures at the time of birth either in the form of face mask ventilation or intubation. Exclusion Criteria: 1. Preterm infants below the threshold of viability as determined by the study team. 2. Major congenital or chromosomal abnormality (including congenital heart disease, Diaphragmatic hernia, congenital pulmonary airway malformations). 3. Severe oligohydramnios (Amniotic fluid index <5 or deep vertical pool=2).

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Carbon dioxide monitoring
Blinded recording of CO2 during preterm resuscitation.

Locations

Country Name City State
United Kingdom James Cook University Hospital Middlesbrough Stockton ON TEES
United Kingdom Imran Ahmed Sunderland

Sponsors (1)

Lead Sponsor Collaborator
South Tees Hospitals NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Factors influencing carbon dioxide levels during preterm resuscitation To study the impact/correlation of various clinical factors (Gestation, Birth weight, need for intubation/bag-mask ventilation, surfactant administration, delayed cord clamping) and resuscitative factors (use of inflation pressures, ventilation pressures, frequency of breaths, face mask ventilation, intubation) on carbon dioxide measurements using MASIMO NOMOLINE capnography during preterm stabilisation. 1 year
Secondary Correlation of Co2 with other parameters Correlation between oxygen saturation, CO2 and pulse rate. 1 year
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