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RecruitingNCT06526091

Cerebral Oxygen Saturation Monitoring During Optimum Cord Management in Preterm Infants

Cerebral Oxygen Saturation Monitoring During Optimum Cord Management in Preterm (COSMIC Pilot Study)

Status
Recruiting
Phase
Study type
Observational
Enrollment
40 (estimated)
Sponsor
Imperial College Healthcare NHS Trust · Academic / Other
Sex
All
Age
1 Minute – 24 Hours
Healthy volunteers

Summary

This study will assess the feasibilty measuring cerebral oxygen saturations using a Near Infrared Spectroscopy (NIRS) monitor immediately after delivery of preterm infants. The investigators aim to evaluate the effects of optimum cord management on cerebral oxygenation in this cohort

Detailed description

Optimal cord management is defined by delaying clamping of the umbilical cord for 1 minute after delivery and is recommend in all neonates, regardless of gestational age. Transfusion of blood from placenta to baby in this minute enables smooth cardiovascular transition and stable cerebral perfusion. Preterm infants are at increased risk of haemodynamic instability and brain injury if the cord is clamped too early. It remains unclear what the optimum time is to clamp the cord in preterm infants, and it is likely different for each baby. Current monitoring of heart rate and peripheral oxygen saturations does not correlate well with oxygen delivery to the brain. Near infrared spectroscopy (NIRS) is a non-invasive method of measuring regional cerebral oxygenation saturations. NIRS may be a helpful monitoring tool to guide optimum timing of cord clamping in preterm infants. This study aims to assess the feasibility of using the INVOS 5100 NIRS monitor immediately after delivery in preterm infants born before 34 weeks gestational age. The investigators aim to assess if they can generate meaningful data on brain oxygen levels in the first few minutes of life. The secondary objectives are to use this data to describe the changes in heart rate, peripheral oxygen and cerebral oxygen saturations during placental transfusion and cord clamping. The investigators will use the INVOS device to measure cerebral oxygenation immediately after delivery, during placental transfusion and cord clamping. We will assess the feasibility of the INVOS device for this purpose. We will use the INVOS data and routinely collected data at delivery to evaluate the effect of optimum cord management on cerebral perfusion, heart rate and peripheral oxygen saturations.

Conditions

Interventions

TypeNameDescription
OTHERCerebral NIRS monitoring at deliveryApplication of cerebral NIRS monitoring immediately after delivery and during optimum cord management

Timeline

Start date
2023-02-15
Primary completion
2024-10-01
Completion
2024-10-01
First posted
2024-07-29
Last updated
2024-07-29

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT06526091. Inclusion in this directory is not an endorsement.