Dose requirement and effect of nicardipine on lipid profile in mild to moderate essential hypertensives

Med J Malaysia. 1992 Sep;47(3):182-9.

Abstract

Twenty eight patients who satisfied the entry criteria and had completed an initial 2 weeks treatment with placebo were titrated fortnightly with doses of Nicardipine ranging from 30 mg to 90 mg daily in two or three divided doses. Nicardipine treatment significantly reduced blood pressures both in the supine and standing positions (p < 0.0004) when compared with placebo treatment. Heart rates however did not change significantly. Forty six percent (13/28) of patients on 20 mg twice daily, 25% (7/28) on 10 mg three times daily, 18% (5/28) of patients on 20 mg three times daily and 11% (3/28) on 30 mg three times daily achieved supine diastolic blood pressures < 90 mm Hg. Nicardipine treatment at 16 weeks and at 24 weeks did not significantly alter the lipid profile when compared to the end of placebo treatment period. No other biochemical abnormalities were reported during the study period. Except for 2 cases of mild pedal oedema and 2 cases of transient headaches, no serious side-effects were encountered.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Blood Pressure / drug effects
  • Cholesterol / blood
  • Female
  • Heart Rate / drug effects
  • Humans
  • Hypertension / blood*
  • Hypertension / physiopathology
  • Lipids / blood*
  • Lipoproteins, HDL / blood
  • Male
  • Middle Aged
  • Nicardipine / administration & dosage*
  • Nicardipine / pharmacology
  • Triglycerides / blood

Substances

  • Lipids
  • Lipoproteins, HDL
  • Triglycerides
  • Cholesterol
  • Nicardipine