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Clinical Trials/CTRI/2024/06/069504
CTRI/2024/06/069504
Not yet recruiting
未知

Efficacy of high flow nasal cannula vs standard Oxygen delivery for management of Transient Tachypnea of New born- A Randomized control trial - nil

none0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: P221- Transient tachypnea of newborn
Sponsor
none
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
none

Eligibility Criteria

Inclusion Criteria

  • gestational age \= 34 weeks admitted within first 6 hours of life.

Exclusion Criteria

  • 1\)Congenital anomalies incompatible with life.
  • 2\)history of thick meconium stained fluid and/or diagnosis of meconium aspiration syndrome
  • 3\)antenatal diagnosis of major congenital pulmonary or cardiac anomalies
  • 4\)initial CXR/ clinical finding demonstrating air leak
  • 5\)Downe score \= 6
  • 6\)Severe Respiratory distress syndrome

Outcomes

Primary Outcomes

Not specified

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