Surfactant Administration by Insure or Thin Catheter
Recruiting
N/A
Interventional Study
RDS of Prematurity
Surfactant Deficiency Syndrome Neonatal
Analgesia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- Up to 2 Days
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 160 (estimated)
- Sponsor
- Karolinska Institutet · Other
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About This Trial
This trial evaluates the efficacy and safety of surfactant administration with thin catheter technique together with analgesic premedication in comparison with the established INSURE-strategy. It will provide valuable knowledge to improve clinical methodology and enhance lung protective treatment strategies for preterm infants.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Infants born before 32 completed weeks of gestation on CPAP, with clinical and radiological signs of RDS and need for surfactant treatment.
Exclusion Criteria:
* Infants requiring surfactant as part of delivery room resuscitation are not eligible.
Infants will be excluded f…
Contacts