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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 8 February 2021
Main ID:  NCT02437552
Date of registration: 29/04/2015
Prospective Registration: Yes
Primary sponsor: University of Sao Paulo
Public title: Cycle Ergometer Exercise in Phase I of Cardiac Rehabilitation After Cardiac Surgery
Scientific title: Cycle Ergometer Exercise in Phase I of Cardiac Rehabilitation After Cardiac Surgery
Date of first enrolment: June 2015
Target sample size: 0
Recruitment status: Withdrawn
URL:  https://clinicaltrials.gov/show/NCT02437552
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Outcomes Assessor).  
Phase:  N/A
Countries of recruitment
Brazil
Contacts
Key inclusion & exclusion criteria

Inclusion Criteria:

- Patients undergoing cardiac surgery type Myocardial Revascularization and Exchange
Mitral Valve Aortic, both sexes and aged between 30-75 years.

Exclusion Criteria:

- Patients undergoing surgical correction of heart disease congenital, aortic aneurysm
and dissection of aorta;

- Present disabling disease to accomplish what is proposed in study as previous
stroke, mental or motor deficit, hearing loss, amputation of the lower limbs
(unilateral or bilateral);

- Present psychomotor agitation of immediate postoperative and first postoperative
and history weaning failure in the immediate;

- Instability hemodynamics and vasoactive drugs;

- Present what other type of peri and postoperative complications;

- Re-operation within 24 hrs.



Age minimum: 30 Years
Age maximum: 70 Years
Gender: All
Health Condition(s) or Problem(s) studied
Cardiac Surgery
Exercise Movement Techniques
Intervention(s)
Device: ergometer cycle exercise
Other: routine physiotherapy
Primary Outcome(s)
Change of six-minute walk test (6MMWT) distance [Time Frame: Before surgery ,third and seventh postoperative day]
Secondary Outcome(s)
Change of spirometric values [Time Frame: Before surgery ,third and seventh postoperative day]
Secondary ID(s)
USP 2015-1
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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