Study of Atenolol Influence on Blood Pressure During Resistance Exercise
NCT ID: NCT01030016
Last Updated: 2009-12-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
10 participants
INTERVENTIONAL
2007-05-31
2009-05-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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NON_RANDOMIZED
CROSSOVER
SUPPORTIVE_CARE
SINGLE
Study Groups
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atenolol
subjects received 6 weeks of atenolol
atenolol
25 mg/day, twice a day for 6 weeks
Interventions
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atenolol
25 mg/day, twice a day for 6 weeks
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* age between 30 and 60 years
* nonobese
Exclusion Criteria
* cardiovascular risk factor
* cardiovascular disease
* physically active
30 Years
60 Years
ALL
No
Sponsors
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Fundação de Amparo à Pesquisa do Estado de São Paulo
OTHER_GOV
University of Sao Paulo
OTHER
Responsible Party
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School of Physical Education and Sport, University of São Paulo
Principal Investigators
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Cláudia LM Forjaz, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Sao Paulo
Decio Mion Jr, PhD
Role: STUDY_CHAIR
University of Sao Paulo
Locations
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University of São Paulo
São Paulo, São Paulo, Brazil
Countries
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Other Identifiers
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FAPESP-06/06356-8
Identifier Type: -
Identifier Source: org_study_id