Skip to main content
OpenTrials
Completed

NCT Number: NCT02739854

Prevalence of Atelectasis in Critical Trauma Patients

The purpose of this study is to identify the prevalence rate and risk factors for pulmonary complications in patients with critical trauma who intubated and mechanical ventilation.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Pulmonary Atelectasis Lung Diseases Respiratory Tract Diseases Wounds and Injuries

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Khon Kaen University

Khon Kaen, 40002, Thailand

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • An inclusion criterion is the traumatic patients (e.g. head injury, blunt chest, blunt abdomen, and fracture of spine; with or without operative, pure or multitrauma) with intubation and mechanical ventilation who admit at this time period will recruit to the study.

Exclusion criteria

  • a patients who admit less than 1 day will be excluded such as sudden death or moving to other ward because of improving conditions, etc.

Treatment and study plan

Primary outcomes

  1. number of participants with pulmonary atelectasis

    Time frame: from the date of randomization until the date of first documented of atelectasis, assessed up to 1 years

Secondary outcomes

  1. number of participants with pneumonia

    Time frame: from the date of randomization until the date of first documented of pneumonia, assessed up to 1 years

  2. number of participants with pleural effusion

    Time frame: from the date of randomization until the date of first documented of pleural effusion, assessed up to 1 years

  3. number of participants with abnormal laboratory values

    Time frame: from the date of randomization until the date of first documented of pleural effusion, assessed up to 1 years

    the laboratory test include arterial blood gases (ABG), Clinical chemistry test (i.e. Blood urea nitrogen, Creatinine, Sodium, Potassium, Phosphorus, Chloride, Magnesium).

  4. number of participants with adverse events that are related to treatment

    Time frame: from the date of randomization until the date of first documented of pleural effusion, assessed up to 1 years

    These data are collected from medical records (i.e. arrhythmia, hypoxia)

Sponsors and collaborators

Lead sponsor

Khon Kaen University

Other

Registry information

Official study title

The Prevalence and Risk Factors for Lung Atelectasis in Patients With Critical Trauma Who Are Intubated and Mechanically Ventilated

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Apr 15, 2016
Registry last updated
Jun 5, 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.

Related clinical trials

Published trials that share one or more normalized conditions with this study.