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N/A N=154 Other

Genetic Determinants of Response to Beta Blockade

Healthy

Enrolled (actual)
154
Serious AEs
0.0%
Results posted
Nov 2018
Primary outcome: Primary: Reduction in Heart Rate — 7.9; 6; 3.3; 9.6 beats per minute

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Atenolol (β-blocker) (Drug)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Vanderbilt University
Primary completion
Dec 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Reduction in Heart Rate
7.9; 6; 3.3; 9.6; 8.4; 7.4

Summary

The overall goal of this project is to determine the genetic factors contributing to interindividual differences in response to beta-blockade.

Eligibility Criteria

Inclusion Criteria

  • Subject must be willing to give written informed consent and be able to adhere to diet and study schedules.
  • Subjects must be free of any clinically significant disease that requires a physician's care and/or would interfere with the study evaluations.
  • Subjects must have a clinically acceptable physical examination and ECG.
  • Laboratory tests (CBC, blood chemistries, and urinalysis) must be within clinically acceptable limits.

Exclusion Criteria

  • Any subject who has taken any prescription or over-the-counter drugs, other than oral contraception if female, within one week prior to study drug administration.
  • Subjects who are presently, or were formerly, narcotic addicts or alcoholics.
  • Active smokers.
  • Subjects who have a clinically significant allergy/intolerance to atenolol.
  • Females with a positive serum/urine pregnancy test at screening.
  • Females who are nursing.
  • Subjects with complete heart block/ any other significant cardiovascular disease.
  • Subjects with a history of asthma symptoms or medication for it within last 10 years.
  • Subjects who have a systolic blood pressure < 90 mm Hg or diastolic blood pressure < 50 mm Hg or heart rate < 50/min at the screening visit or on the baseline pre drug values on the study day.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00837902). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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