Cerebral Oxygen Saturation Monitoring During Optimum Cord Management in Preterm Infants
Recruiting
Observational Study
Pre-Term
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 1 Minute – 24 Hours
- Sex
- Any
- Study type
- Observational
- Participants needed
- 40 (estimated)
- Sponsor
- Imperial College Healthcare NHS Trust · Other
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About This Trial
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
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* All babies eligible for optimum cord management born before 34 completed weeks gestational age
* Parental consent
Exclusion Criteria:
* Multiple pregnancies
* Infants for whom resuscitation at birth is not appropriate
* Antenatal or immediate postnatal diagnosis of severe co…
Contacts