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OpenTrials
Completed

NCT Number: NCT00866255

Continuous Measurement of Intratracheal Pressure

Continuous measurement of intratracheal pressure in mechanically ventilated infants using a fibreoptic pressure transducer in the endotracheal tube (ETT). Based on the findings, tracheal pressure can continuously be monitored in the presence of pediatric ETTs by combining ETT coefficients and the flow and airway pressure continuously measured at the proximal end of the ETT.

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Key information

Age range

1 day–10 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Medical Center Freiburg

Freiburg im Breisgau, 79106, Germany

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Children < 10 Years
  • volume-controlled ventilation

Exclusion criteria

  • refusal of written informed consent
  • severe pulmonary diseases

Treatment and study plan

endotracheal tube pressure measurement probe

Device

The endotracheal tube pressure measurement probe is inserted into the endotracheal tube prior to intubation for measurement of tracheal pressure at the tip of the endotracheal tube.

Primary outcomes

  1. tracheal pressure

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

University Hospital Freiburg

Other

Registry information

Official study title

Continuous Measurement of Intratracheal Pressure in Mechanically Ventilated Infants

Important dates

Study start
2008
Primary completion
2009
First posted
Mar 20, 2009
Registry last updated
Feb 2, 2010

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.