The study is a non-pharmacological interventional, single-center, national, non-randomised, comparative and open label.
The study is carried out to evaluate primarily the difference in the activity of the renal transporter ENaC (through dosage of sodium) through its inhibition with a single dose of Amiloride in hypertensive patients characterized by the polymorphism of alpha Adducin rs496. It's also aimed to see the difference in potassium and the change in systolic and diastolic blood pressure after amiloride administration
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
40
administration of a single dose of 5 or 10 mg of Amiloride (based on body weight) After oral intake of the drug, the increase in sodium in the urine ends within 8 hours
San Raffaele Hospital
Milan, Lombardy, Italy
Evaluate urinary sodium
Evaluation of sodium levels after oral administration of Amiloride
Time frame: 3 hrs and 6 hrs
Evaluate potassium levels
Evaluation of potassium plasma levels after oral administration of Amiloride
Time frame: 3 hrs and 6 hrs
Evaluation of systolic blood pressure
Evaluation of systolic blood pressure after oral administration of Amiloride
Time frame: 3 hrs and 6 hrs
Evaluation of diastolic blood pressure
Evaluation of diastolic blood pressure after oral administration of Amiloride
Time frame: 3 hrs and 6 hrs
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