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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01967108
Other study ID # 0346-13-RMB CTIL
Secondary ID
Status Completed
Phase N/A
First received October 17, 2013
Last updated May 6, 2015
Start date December 2013
Est. completion date March 2015

Study information

Verified date February 2014
Source Rambam Health Care Campus
Contact n/a
Is FDA regulated No
Health authority Israel: The Israel National Institute for Health Policy Research and Health Services Research
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine the efficacy of chest physiotheray treatment in preventing pulmonary complications and weaning faliure, in extubated critically ill patients.


Recruitment information / eligibility

Status Completed
Enrollment 65
Est. completion date March 2015
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:ICU patients, over 18 years' old, mechanical ventilated over 24 hours, candidates for extubation -

Exclusion Criteria: Mental conditions, retardation, dementia, pregnancy, re-intubated patients

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Weaning From Mechanical Ventilation

Intervention

Other:
chest physiotherapy
chest physiotherapy, up to one hour from extubation, in ICU patients

Locations

Country Name City State
Israel Intensive Care Unit, Rambam Health Care Campus Haifa

Sponsors (1)

Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary re-intubation re-intubation up to 48 hours post extubation will be considered a weaning failure 48 hours No
Secondary oxygen saturation decrease 48 hours No
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