The Effect of Surfactant Administration on Cerebral Oxygenation

Zekai Tahir Burak Women's Health Research and Education Hospital

Status: Suspended

Conditions: Prematurity; Respiratory Distress Syndrome

Treatments: Device: near infrared spectroscopy (INVOS 5100)

Study type: Observational

Funder types: Other

Identifiers

NCT01258517

NIRS-018

Details and patient eligibility

About

The purpose of this study is to assess changes in cerebral oxygenation during two different types (beractant and poractant) and two different routes (double lumen or single lumen endotracheal tube) of surfactant administration using near infrared spectroscopy (NIRS).

Enrollment: 40 estimated patients

Sex: All

Ages: 23 to 32 weeks old

Volunteers: No Healthy Volunteers

Inclusion criteria

Clinical diagnosis of respiratory distress syndrome <32 gestational weeks and/or <1500 g birthweight

Exclusion criteria

major congenital anomalies complex congenital heart diseases

Trial design

40 participants in 1 patient group

group 1, group 2, group 3, group 4

Description:

administration of beractant with single lumen ET tube administration of poractant with single lumen ET tube administration of beractant with double lumen ET tube administration of poractant with double lumen ET tube

Treatment:

Device: near infrared spectroscopy (INVOS 5100)