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Post Extubation Chest Physiotherapy in ICU

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ClinicalTrials.gov Identifier: NCT01967108
Recruitment Status : Completed
First Posted : October 22, 2013
Last Update Posted : May 7, 2015
Sponsor:
Information provided by (Responsible Party):
Rambam Health Care Campus

Brief 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.

Condition or disease Intervention/treatment Phase
Weaning From Mechanical Ventilation Other: chest physiotherapy Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 65 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: The Effect of Post Extubation Chest Physiotherapy on Respiratory Complications and Weaning Failure in Critically Ill Patients
Study Start Date : December 2013
Actual Primary Completion Date : March 2015
Actual Study Completion Date : March 2015

Arm Intervention/treatment
Experimental: chest physiotherapy
chest physiotherapy in patient's bed, including deep breathing, directed cough, arm movment and more.
Other: chest physiotherapy
chest physiotherapy, up to one hour from extubation, in ICU patients

No Intervention: control group
This patients will not recive chest physiotherapy after extubation, unless developing respiratory deterioration



Primary Outcome Measures :
  1. re-intubation [ Time Frame: 48 hours ]
    re-intubation up to 48 hours post extubation will be considered a weaning failure


Secondary Outcome Measures :
  1. oxygen saturation decrease [ Time Frame: 48 hours ]


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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

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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01967108


Locations
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Israel
Intensive Care Unit, Rambam Health Care Campus
Haifa, Israel
Sponsors and Collaborators
Rambam Health Care Campus
Investigators
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Principal Investigator: Enbar Foox, B.PT Rambam Health Care Campus

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Responsible Party: Rambam Health Care Campus
ClinicalTrials.gov Identifier: NCT01967108     History of Changes
Other Study ID Numbers: 0346-13-RMB CTIL
First Posted: October 22, 2013    Key Record Dates
Last Update Posted: May 7, 2015
Last Verified: February 2014