Pre- and Postoperative Cardiopulmonary Rehabilitation Reduces Complications After Coronary Artery Bypass Surgery: A Randomized Trial

This study has been completed.
Sponsor:
Collaborator:
ICSC
Information provided by:
Universidade do Sul de Santa Catarina
ClinicalTrials.gov Identifier:
NCT00670176
First received: April 29, 2008
Last updated: April 30, 2008
Last verified: April 2008

April 29, 2008
April 30, 2008
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length of stay in the ICU (in minutes); days on the ward after ICU until hospital discharge; pneumonia with the need for antibiotic treatment; and atrial fibrillation or flutter detected on daily-performed electrocardiograms
Same as current
Complete list of historical versions of study NCT00670176 on ClinicalTrials.gov Archive Site
time until oro-tracheal tube (OTT) removal, occurrence of pleural effusion, atelectasis, change in peak-flow (baseline vs. 2 hours after extubation vs. discharge), and changes in the 6-minute-walking distance between enrollment and hospital discharge.
Same as current
Not Provided
Not Provided
 
Pre- and Postoperative Cardiopulmonary Rehabilitation Reduces Complications After Coronary Artery Bypass Surgery: A Randomized Trial
Pre- and Postoperative Cardiopulmonary Rehabilitation Reduces Complications After Coronary Artery Bypass Surgery: A Randomized Trial

Pre- and postoperative cardiopulmonary rehabilitation reduces complications after coronary artery bypass surgery. This study was conducted as a randomized trial to verify this hypothesis in our institution. ICSC

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Prevention
Coronary Artery Bypass Surgery
Behavioral: REHAB (Pre- and postoperative cardiopulmonary rehabilitation)
Experimental: I
Intervention: Behavioral: REHAB (Pre- and postoperative cardiopulmonary rehabilitation)
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
56
June 2005
Not Provided

Inclusion Criteria:

  • All CAB patients

Exclusion Criteria:

  • SCA in the previous 24h and incapacity of doing light exercise. Valvular patients
Both
Not Provided
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT00670176
ICSC01
Yes
Not Provided
Universidade do Sul de Santa Catarina
ICSC
Not Provided
Universidade do Sul de Santa Catarina
April 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP