Hôpital Louis Pradel
Bron, 69677, France
NCT Number: NCT00128518
The principal scientific objective of the trial is to identify the factors that are associated with differential blood pressure responses between drugs. This may allow investigators to produce new hypotheses on the pathophysiology of hypertension and on the mechanisms of drug action.
These factors can be of different types:
* Environmental factors (sodium or alcohol intake); * Morphological (height, weight, body mass index, body surface area); * Initial blood pressure; * Electrocardiogram (ECG) parameters of left ventricular hypertrophy; * Biological parameters as the activity level of the renin angiotensin aldosterone system; * Genetic polymorphisms.
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Notify Me25 year–60 year
All sexes
Interventional
Phase 4
Bron, 69677, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
1.5 mg/day during 4 weeks
4 mg/day during 1 week then 8 mg/day during 3 weeks
1 pill/day during 1 week then 2 pills/day during 3 weeks
1 pill/day during 4 weeks
Time frame: 16 weeks
Change from baseline and after each 4 week treatment period
Hospices Civils de Lyon
Other
IDEAL Study : Identification of the Determinants of the Efficacy of Arterial Blood Pressure Lowering Drugs
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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