N/A
N=154
Genetic Determinants of Response to Beta Blockade
Healthy
Bottom Line
View on ClinicalTrials.gov: NCT00837902 ↗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
| Outcome | Result | p-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.
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.