MedTrace Logo

The Effect of Surfactant Administration on Cerebral Oxygenation

NCT01258517 · Status: SUSPENDED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2016-09-05

No results posted yet for this study

Summary

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).

Conditions

  • Respiratory Distress Syndrome
  • Prematurity

Interventions

DEVICE

near infrared spectroscopy (INVOS 5100)

monitorization of cerebral oxygenation by INVOS 5100 during surfactant administration

Sponsors & Collaborators

  • Zekai Tahir Burak Women's Health Research and Education Hospital

    lead OTHER

Eligibility

Min Age
23 Weeks
Max Age
32 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2018-06-30
Completion
2018-12-31

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01258517 on ClinicalTrials.gov