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Clinical Trial Summary

Prospective study comparing hemodynamic and respiratory changes and exercise capacity during Cardio-Pulmonary-Exercise-Testing (CPET) in 4 groups of infants; Three different groups of premature infants and term controls


Clinical Trial Description

The study population included 4 groups of infants; preterm infants born < 300 weeks' gestation with BPD (i.e. oxygen dependence for at least 28 postnatal days 5), preterm infants born < 300 weeks' gestation without BPD, late preterm infants (born at 340-366 weeks' gestation) and term controls. Pulmonary function testing and spirometry were measured Participants performed CPET on an electronically braked cycle ergometer. During the exercise testing, serial saturation, heart rate and blood pressure measurements were obtained. The peak oxygen consumption (VO2max) was measured and served as the primary endpoint of the study. ;


Study Design


Related Conditions & MeSH terms

  • Premature Birth
  • The Peak Oxygen Consumption (VO2max) Was Measured and Served as the Primary Endpoint of the Study

NCT number NCT04833647
Study type Interventional
Source Rambam Health Care Campus
Contact
Status Completed
Phase N/A
Start date April 1, 2016
Completion date February 1, 2021