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Clinical Trials/IRCT201709049014N181
IRCT201709049014N181
Recruiting
Phase 2

Comparison of the efficacy and complication of humidified high flow nasal cannula versus nasal continuous positive airway pressure after treatment with surfactant in neonate with respiratory distress syndrome: a randomized clinical trial

Vice-chancellor for Research and Technology, Hamadan University of Medical Sciences0 sites60 target enrollmentTBD
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ConditionsAdult respiratory distress syndrome.Adult respiratory distress syndrome

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Adult respiratory distress syndrome.
Sponsor
Vice-chancellor for Research and Technology, Hamadan University of Medical Sciences
Enrollment
60
Status
Recruiting
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Vice-chancellor for Research and Technology, Hamadan University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • •Age of 28 to 36 months; premature neonate; affecting with respiratory distress syndrome; hospitalization in NICU with 24 hours after birth.
  • •Exclusion criteria: Being born in other hospitals.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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