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NCT02283138 Clinical Trial

Prediction of Neonatal Respiratory Distress Syndrome in Preterm Fetuses by Assessment of Fetal Lung Volume by Vocal and Pulmonary Artery Resistance Index a Pilot Study

Fetal Lung Volume of Preterm Fetuses Measured by VOCAL, PA-RI Measured by Pulsed Doppler Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02283138
Other study ID # lab7680
Secondary ID
Status Completed
Phase N/A
First received October 31, 2014
Last updated July 16, 2017
Start date November 2014
Est. completion date July 2017

Study information
Verified date July 2017
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators will measure fetal lung volume by VOCAL and pulmonary artery resistance index in preterm fetuses and correlating the results with postnatal respiratory distress of the preterm neonates.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date July 2017
Est. primary completion date March 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- preterm labour

Exclusion Criteria:

- twins

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Egypt Ain Shams Maternity Hospital Cairo

Sponsors (2)
Lead Sponsor Collaborator
Ain Shams University Ain Shams Maternity Hospital

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Neonatal respiratory distress Apgar score at birth, need for NICU admission after delivery, need for neonate with RDS for continuous positive airway pressure ventilation at time of delivery
Secondary Neonatal mortality rate Follow up for early neonatal mortality rate after NICU admission , One week after delivery