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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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28 November 2016 |
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Main ID: |
NCT02965365 |
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Date of registration:
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13/11/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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PATET Ratio to Rule Out Transient Tachypnea of the Newborn
PATET |
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Scientific title:
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A Non-invasive Method To Rule Out Transient Tachypnea of the Newborn (TTN) : Pulmonary Artery Acceleration to Ejection Time Ratio |
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Date of first enrolment:
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January 2016 |
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Target sample size:
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105 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02965365 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Phase:
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N/A
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Countries of recruitment
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Turkey
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Contacts
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Name:
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Baris Büke, resident |
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Address:
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Telephone:
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Email:
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Affiliation:
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Kayseri Education and Research Hospital |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Singleton pregnancies who delivered beyond 34 weeks gestational age
Exclusion Criteria:
- fetal abnormality, chronicle maternal disease, pregnancy complication (preeclampsia,
diabetes, intrauterine growth restriction,etc.)
Age minimum:
18 Years
Age maximum:
35 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Transient Tachypnea of the Newborn
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Primary Outcome(s)
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PATET ratio
[Time Frame: 5 minutes]
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Secondary Outcome(s)
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PA PI
[Time Frame: 2 minutes]
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Secondary ID(s)
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E52332816_54
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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