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Clinical Trials/NCT01939509
NCT01939509CompletedPhase 4

Comparison of the Hemodynamic Changes in Patients Under Treatment With Bisoprolol Versus Atenolol

Hospital Italiano de Buenos Aires1 site in 1 country80 target enrollmentStarted: February 2012Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
80
Locations
1
Primary Endpoint
central blood pressure

Study Overview

Brief Summary

At hemodynamic level, the greater affinity of bisoprolol by the beta 1 receptor in theory could improve the peripheral arterial perfusion and could have a greater antihypertensive effect. At the same time, this could carry objectifiable improvements in the vascular tree, such as the level of arterial stiffness.

This study attempts to mark the hemodynamic differences in the same individual with hypertension and metabolic syndrome who will be exposed to both drugs at different moments. Parameters will be objectified with impedance cardiography, pulse wave velocity and central blood pressure assessment before and after taking each one of the drugs. The results will be compared to the baseline data and between themselves.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Hypertension
  • Metabolic syndrome

Exclusion Criteria

  • Severe hypertension >180/110
  • Secondary hypertension
  • Contraindication for betablockers
  • Prior treatment with betablockers (up to one month before inclusion)
  • History of neoplastic disease
  • Patients that do not sign informed consent

Arms & Interventions

Atenolol-Bisoprolol

Experimental

Intervention: Atenolol (Drug)

Atenolol-Bisoprolol

Experimental

Intervention: Bisoprolol (Drug)

Outcomes

Primary Outcomes

central blood pressure

Time Frame: two months

Secondary Outcomes

  • cardiac index(two months)
  • pulse wave velocity(two months)
  • peripheral resistance(two months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lucas Aparicio

MD

Hospital Italiano de Buenos Aires

Study Sites (1)

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