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OpenTrials
Completed

NCT Number: NCT02309190

Transpulmonary Pressures in Mechanical Ventilated Patients With Morbid Obesity

The study consists in determine the transpulmonary pressure in morbidly obesity patients that require mechanical ventilation.

* both gender * only adults * Medical intensive care patients.

Completed

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

The University of Texas - HSC at Houston

Houston, Texas, 77030, United States

About this study

We are studying adult patients with morbid obesity with respiratory failure requiring mechanical ventilation.

We are measuring transesophageal presssures to estimate ideal PEEP and evaluate hemodynamic parameters.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • both gender
  • morbid obesity
  • hemodynamically stable

Exclusion criteria

  • pregnant patients
  • cirrhotic patients with esophageal varicose

Treatment and study plan

Primary outcomes

  1. Transpulmonary pressure

    Time frame: one year

    We will record the changes in transpulmonary pressure after adjusting PEEP (measure in cmH2O).

Secondary outcomes

  1. hemodynamics

    Time frame: one year

    we will review hemodynamic changes while adjusting PEEP (BP, HR).

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center, Houston

Other

Registry information

Important dates

Study start
2018
Primary completion
2024
Study completion
2024
First posted
Dec 5, 2014
Registry last updated
Dec 12, 2024

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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