Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03008200
Other study ID # KayseriEAH
Secondary ID
Status Completed
Phase N/A
First received December 20, 2016
Last updated December 31, 2016
Start date December 2015
Est. completion date September 2016

Study information

Verified date December 2016
Source Kayseri Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority Turkey: Ministry of Health
Study type Observational

Clinical Trial Summary

Fetal PATET ratio evaluation to predict neonatal RDS


Description:

115 patients were enrolled in this study.Population was recruited from singleton pregnancies beyond 27 weeks of gestation.All participants underwent a ultrasound examination to measure fetal pulmonary artery acceleration to ejection time ratio (PATET) by a single experienced clinician. After the delivery respiratory distress diagnosis made by a pediatrician who were blinded the doppler waveform measurements.Following the diagnosis, neonates divided into 2 groups as RDS (+) and RDS (-). In addition of RDS diagnosis, neonatal features like 1st and 5th minute APGAR scores, neonatal intensive care unit (NICU) admission and duration in NICU were also recorded. Afterwards all parameters were statistically analyzed if there is any significant differences between those two groups.


Recruitment information / eligibility

Status Completed
Enrollment 115
Est. completion date September 2016
Est. primary completion date September 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- pregnant women within the 27 weeks of gestation and beyond

Exclusion Criteria:

- patients who did not give birth within 3 days after the ultrasonographic doppler examination

- fetuses with Any congenital abnormalities

- amniotic fluid abnormalities

- any chronic maternal diseases or pregnancy complications such as;gestational diabetes mellitus,preeclampsia

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • RDS
  • Respiratory Distress Syndrome, Adult
  • Respiratory Distress Syndrome, Newborn

Intervention

Device:
ultrasound examination
intrauterine fetal pulmonary artery acceleration time to ejection time ratio measurement via ultrasound

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Kayseri Education and Research Hospital

References & Publications (3)

Azpurua H, Norwitz ER, Campbell KH, Funai EF, Pettker CM, Kleine M, Bahtiyar MO, Malkus H, Copel JA, Thung SF. Acceleration/ejection time ratio in the fetal pulmonary artery predicts fetal lung maturity. Am J Obstet Gynecol. 2010 Jul;203(1):40.e1-8. doi: 10.1016/j.ajog.2010.01.075. — View Citation

Guan Y, Li S, Luo G, Wang C, Norwitz ER, Fu Q, Tu X, Tian X, Zhu J. The role of doppler waveforms in the fetal main pulmonary artery in the prediction of neonatal respiratory distress syndrome. J Clin Ultrasound. 2015 Jul-Aug;43(6):375-83. doi: 10.1002/jcu.22219. — View Citation

Schenone MH, Samson JE, Jenkins L, Suhag A, Mari G. Predicting fetal lung maturity using the fetal pulmonary artery Doppler wave acceleration/ejection time ratio. Fetal Diagn Ther. 2014;36(3):208-14. doi: 10.1159/000358299. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Measurement of fetal pulmonary acceleration time to ejection time ratio via ultrasonography in the 115 pregnant women between 27 to 37 weeks of gestation for prediction of respiratory distress syndrome The aim of this study is to obtain the effectiveness of fetal pulmonary artery acceleration time to ejection time ratio in fetal lung maturity evaluation Ten months No
See also
  Status Clinical Trial Phase
Completed NCT01517958 - Lung Ultrasound to Diagnose Transient Tachypnea of the Newborn (TTN) Versus Respiratory Distress Syndrome (RDS) in Neonates N/A
Not yet recruiting NCT02571231 - High Flow Ventilation With Volume Guarantee N/A
Not yet recruiting NCT04820101 - Dexmedetomidine for LISA Procedure in Preterm Infants N/A
Completed NCT02076126 - Determination of Lung Maturity and Prediction of RDS at Birth N/A
Not yet recruiting NCT01265589 - Intratracheal Vitamin A Administration With Surfactant for Newborn Respiratory Distress Syndrome Phase 3
Completed NCT01511952 - A Multi-Site Study of Music Therapy Interventions on Vitals, Feeding and Sleep in Premature Infants N/A
Recruiting NCT05493527 - Noninvasive High Frequency Oscillatory Ventilation as a Post-extubation Respiratory Support in Neonates N/A
Completed NCT01942473 - Effects of Automated Adjustment of FiO2 on Cerebral and Arterial Oxygenation in Preterm Infants N/A
Recruiting NCT03217162 - Surfactant for Neonate With Acute Respiratory Distress Syndrome (ARDS) N/A