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Published on: May 26, 2022
[Captopril in single doses in the treatment mild-moderated arterial hypertension]
J Alcántara Nicolás1, R Cano Cano, E Cano Cano
1GRAMU, Unidad de Hipertensión Hospitalaria, Murcia.
Insights
Single-dose Captopril effectively treats mild to moderate essential hypertension. Combining Captopril with hydrochlorothiazide significantly improves blood pressure control in hypertensive patients.
Area of Science:
- Cardiology
- Pharmacology
- Hypertension Research
Background:
- Essential arterial hypertension is a prevalent condition requiring effective management.
- Early intervention with antihypertensive medications is crucial for preventing cardiovascular complications.
Purpose of the Study:
- To evaluate the efficacy and tolerance of single-dose Captopril, alone and in combination with hydrochlorothiazide, for treating mild to moderate essential hypertension.
Main Methods:
- A multicentric study involving 88 patients with mild to moderate essential hypertension.
- Patients received varying regimens: single-dose Captopril, or Captopril combined with hydrochlorothiazide.
- Blood pressure was monitored over a minimum 4-month follow-up period.
Main Results:
- Single-dose Captopril achieved a 53.4% response rate.
- Combination therapy with hydrochlorothiazide significantly increased response rates to over 89%.
- Statistically significant blood pressure reduction (mean 14%) was observed with both monotherapy and combination therapy.
Conclusions:
- Single-dose Captopril is a useful and well-tolerated initial treatment for mild to moderate essential hypertension.
- Combination therapy with hydrochlorothiazide enhances blood pressure control.
- The treatment demonstrated good tolerance with minimal adverse effects.
Abstract:
The effect of single dose (50 mg) Captopril (C) used either alone or associated to diuretics (50 mg hydrochlorothiazide -HCTI) in the treatment of mild-moderate essential arterial hypertension was studied in a multicentric study. Eighty eight patients were chosen. After a minimum of 4 month follow-up period 53.4% responded (BDP less than 95 mm Hg) to single dose C (group 1:47 patients), 89.77% to 50 mg C in single dose together with 50 mg HTIT (group 2: 32 patients), 95.45% of two 50 mg doses of C and 50 mg HCIT (group 3: 5 patients), and 97.72% responded to 3 doses of C and 50 mg of HCTI (group 4: 2 patients). The decrease in blood pressure values was statistically significant (p, 000, Wilcoxon test) in groups 1 and 2, having a mean decrease in blood pressure (BP) of 14%. In group 1 (n = 42) the SBP which initially was 165.72 +/- 11.32, decreased to 148.28 +/- 11.5 and the DBP decreased from 101.55 +/- 5.68 to 87.28 +/- 6.59. In group 2 (n = 32) the SBP decreased from 173.50 +/- 14.08 to 152.44 +/- 20.8 and the DBP from 103.34 +/- 5.29 to 87.47 +/- 6.39. The response to monotherapy could not be statistically correlated either to early essential hypertension or to the patients age. Treatment was discontinued in three cases due to the secondary effects, cough, ageusia and nervousness, showing the remaining patients a good tolerance. No changes were observed in the analytical parameters. This study shows the usefulness and tolerance of single dose C as the initial treatment of mild to moderate essential hypertension.
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