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OpenTrials
Completed

NCT Number: NCT04936477

Ventilation-perfusion (V/Q) Ratio and Alveolar Surface Area in Preterm Infants

To non-invasively estimate the alveolar surface area of the lungs of prematurely born infants by taking measurements of oxygen and carbon dioxide and utilizing functional morphometry.

Completed

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Key information

Age range

22 week–28 week

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

King's College Hospital NHS Foundation Trust

London, United Kingdom

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

-

Exclusion criteria

  • Congenital or chromosomal anomalies

Treatment and study plan

Calculation of ventilation-perfusion ratio

Other

Three to five paired measurements of fraction of inspired oxygen and peripheral oxygen saturations.

Insertion of mainstream capnograph with combined pressure and flow sensor to perform end-tidal capnography measurement.

Echocardiogram to assess intra-cardiac shunting.

Primary outcomes

  1. Calculation of the alveolar surface area in prematurely born infants using validated functional morphometry

    Time frame: One year

Sponsors and collaborators

Lead sponsor

King's College London

Other

Collaborators

  • King's College Hospital NHS Trust

Registry information

Official study title

Functional Morphometry and Ventilation Perfusion Ratio to Estimate the Alveolar Surface Area in Prematurely Born Infants

Important dates

Study start
2020
Primary completion
2022
Study completion
2023
First posted
Jun 23, 2021
Registry last updated
Mar 17, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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