G. Honos et al., ONCE-DAILY PERINDOPRIL VERSUS SLOW-RELEASE DILTIAZEM IN THE TREATMENTOF MILD-TO-MODERATE ESSENTIAL-HYPERTENSION, Canadian journal of cardiology, 10, 1994, pp. 8-12
The efficacy and acceptability of the angiotensin-converting enzyme (A
CE) inhibitor perindopril were compared with those of an established t
reatment for hypertension in Canada, slow release diltiazem. Hypertens
ive patients aged 18 to 64 years presenting a mean sitting diastolic b
lood pressure (DBP) between 95 and 110 mmHg inclusive were randomized
if they were without any concurrent serious renal, hepatic, cardiac or
psychiatric illnesses. A total of 49 of 83 patients qualified for ran
domization after four weeks on placebo, 23 were assigned to the perind
opril treatment group and 26 to the diltiazem treatment group. Startin
g doses (4 mg od in the perindopril group and 120 mg [60 mg bid] in th
e diltiazem group) were increased to a maximum of 8 mg od in the perin
dopril group and to 360 mg (180 mg bid) in the diltiazem group if DBF
remained above 90 mmHg. Hydrochlorothiazide was added at week 8 if goa
l blood pressure was not achieved with the maximum dose. Both groups w
ere comparable at randomization; baseline systolic blood pressure (SGP
)/DBP were 153/100 mmHg and 150/99 mmHg in the perindopril and diltiaz
em groups, respectively. A significant decrease in SBP/DBP was observe
d from the second week of treatment: -10/-8 mmHg in the perindopril gr
oup and -8/-8 mmHg in the diltiazem group. This fall in blood pressure
was maintained throughout the duration of the trial: -13/-9 and -13/-
11 mmHg for the perindopril and diltiazem groups, respectively, at wee
k 12, at which time monotherapy was taken by over 80% of patients and
compliance was consistently over 90%. One patient treated with perindo
pril withdrew before the end of the trial due to depression associated
with personal problems. Systematic questioning about an exhaustive li
st of 11 symptoms at all visits showed no significant trends and no se
rious events. There were no significant changes in any laboratory para
meters. Both drugs had a neutral effect on serum lipids, glucose, seru
m markers of kidney and renal function and on hematological parameters
. In conclusion, this Canadian multicentre trial confirmed that the ef
ficacy and acceptability of the once daily ACE inhibitor perindopril,
administered in a simple dosing scheme of 4 to 8 mg, is equivalent to
that of slow release diltiazem in the treatment of hypertension.