Pre- and Postoperative Cardiopulmonary Rehabilitation Reduces Complications After Coronary Artery Bypass Surgery: A Randomized Trial
This study has been completed.
Sponsor:
Universidade do Sul de Santa Catarina
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
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Purpose
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
| Condition | Intervention |
|---|---|
|
Coronary Artery Bypass Surgery |
Behavioral: REHAB (Pre- and postoperative cardiopulmonary rehabilitation) |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Pre- and Postoperative Cardiopulmonary Rehabilitation Reduces Complications After Coronary Artery Bypass Surgery: A Randomized Trial |
Resource links provided by NLM:
Further study details as provided by Universidade do Sul de Santa Catarina:
Primary Outcome Measures:
- 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
Secondary Outcome Measures:
- 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.
| Estimated Enrollment: | 56 |
| Study Completion Date: | June 2005 |
| Arms | Assigned Interventions |
|---|---|
| Experimental: I | Behavioral: REHAB (Pre- and postoperative cardiopulmonary rehabilitation) |
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- All CAB patients
Exclusion Criteria:
- SCA in the previous 24h and incapacity of doing light exercise. Valvular patients
Contacts and Locations
No Contacts or Locations Provided
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00670176 History of Changes |
| Other Study ID Numbers: | ICSC01 |
| Study First Received: | April 29, 2008 |
| Last Updated: | April 30, 2008 |
| Health Authority: | Brazil: National Committee of Ethics in Research |
ClinicalTrials.gov processed this record on May 21, 2013