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Phase 4 N=888 Randomized Treatment

Pharmacogenomic Evaluation of Antihypertensive Responses

Hypertension

Enrolled (actual)
888
Serious AEs
0.5%
Results posted
Jul 2013
Primary outcome: Primary: Blood Pressure Response (Delta BP (After 18 Weeks of Medication - Baseline)). — -12.06; -13.33 mmHg

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Hydrochlorothiazide (Drug); Atenolol (Drug)
Age
Pediatric, Adult, Older Adult · 17+ yrs
Sex
All
Sponsor
University of Florida
Primary completion
Dec 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Blood Pressure Response (Delta BP (After 18 Weeks of Medication - Baseline)).
-12.06; -13.33
SECONDARY
Adverse Metabolic Responses

Summary

There are many medications available for the treatment of high blood pressure (hypertension), but finding the right one for a specific patient can be challenging. In fact, it is estimated that only 34% of people with hypertension have their blood pressure under control. The hypothesis is that genetic differences between individuals influence their response to antihypertensive medications. This study is aimed at determining the genetic factors that may influence a person's response to either a beta-blocker or a thiazide diuretic. The hope is that through this research, we may someday be able to use an individual's genetic information to guide the selection of their blood pressure medicine, leading to better control of blood pressure, and less need for the current trial and error process.

Eligibility Criteria

Inclusion Criteria

An average seated home diastolic blood pressure (DBP) > 85 mmHg and home systolic blood pressure (SBP) 5 minutes) clinic DBP between 90 mmHg and 110 mmHg and SBP 1.5 in men or 1.4 in women), primary renal disease, pregnancy or lactation, liver enzymes > 2.5 upper limits of normal, current treatment with NSAIDS, cyclooxygenase-2 (COX2) inhibitors, oral contraceptives or estrogen.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00246519). 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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