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OpenTrials
Completed

NCT Number: NCT01885793

Cuff Pressure in Patients: Manometer vs Invasive Pressure Monitoring Setup

This is a prospective study looking at ways to measure the cuff pressure of cuffed endotracheal tubes (ETTs). We will be comparing a hand-held manometer (MM) to the transducer of an invasive pressure monitoring setup (IPMS), which is commonly used for arterial or central venous pressure monitoring. The investigators previously did this study in vivo with ETTs in polyvinyl chloride (PVC) "tracheas" and we found that there is good correlation between the pressure readings using the MM and the IPMS. The purpose of the current study is to validate the in vitro findings in clinical situations.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Nationwide Children's Hospital

Columbus, Ohio, 43205, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Intubation of trachea with a cuffed endotracheal tube.

Exclusion criteria

  • None

Treatment and study plan

Cuffed endotracheal tube

Device

Intubation with a cuffed endotracheal tube (ETT).

Primary outcomes

  1. Intracuff pressure

    Time frame: Immediately after intubation

    Intracuff pressure is measured via handheld manometer and by using the transducer of an invasive pressure monitoring device.

Sponsors and collaborators

Lead sponsor

Senthil G. Krishna

Other

Registry information

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Jun 25, 2013
Registry last updated
Jan 31, 2017

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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