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Published on: May 26, 2022
Introducing candesartan 32 mg plus hydrochlorothiazide 25 mg in previously untreated patients with severe essential
Peter Baumgart1, Ingomar Naudts2, Gerhard Kiel3
1Clemenshospital Muenster, Academic Teaching Hospital of University of Muenster, Germany.
Insights
This study shows that a stepped treatment with candesartan and hydrochlorothiazide effectively lowers blood pressure in severe hypertension. The combination therapy achieved significant reductions, with over 50% of patients reaching target blood pressure levels.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Severe essential hypertension requires effective treatment strategies.
- Combination therapy is often necessary to achieve blood pressure control.
Purpose of the Study:
- To evaluate the efficacy and safety of a stepped-care approach using candesartan and hydrochlorothiazide (HCTZ) in patients with severe essential hypertension.
- To determine the effectiveness of escalating doses of candesartan and HCTZ in achieving target blood pressure.
Main Methods:
- Prospective, open-label, single-group study involving 106 treatment-naive patients with severe hypertension.
- Patients initiated on candesartan 16 mg, followed by addition of HCTZ 12.5 mg, and finally escalated to candesartan 32 mg/HCTZ 25 mg over 9 weeks.
- Primary endpoint: mean reduction in systolic blood pressure (SBP) and diastolic blood pressure (DBP); response defined as SBP <140 mmHg or ≥20 mmHg decrease, and DBP <90 mmHg or ≥10 mmHg decrease.
Main Results:
- Significant reductions in SBP (44.4 ± 16.8 mmHg) and DBP (32.0 ± 11.3 mmHg) were observed (P < 0.0001).
- Overall response rate was 92.4%, with 64.8% of patients achieving blood pressure <140/90 mmHg.
- The target blood pressure of <140/90 mmHg was achieved by over 50% of patients only after the full dose titration of candesartan 32 mg/HCTZ 25 mg.
Conclusions:
- A stepped treatment approach with candesartan/HCTZ combination therapy is effective and safe for rapid blood pressure reduction in newly diagnosed severe hypertension.
- Achieving the target blood pressure of <140/90 mmHg requires the full therapeutic dose of candesartan 32 mg and HCTZ 25 mg in a significant proportion of patients.
Purpose:
To investigate the efficacy of candesartan 32 mg and hydrochlorothiazide (HCTZ) 25 mg combination in patients with severe essential hypertension.
Patients And Methods:
In this prospective, open-label, single-group study, 106 previously untreated patients with a baseline systolic blood pressure (SBP) of 150-200 mmHg, and a diastolic blood pressure (DBP) of 110 to 120 mmHg, started with candesartan 16 mg during the first week. HCTZ 12.5 mg was added at week 2 and from fourth week onwards candesartan 32 mg plus HCTZ 25 mg was given over 6 weeks. The primary efficacy endpoint was mean reduction in SBP and DBP after 9 weeks. Response was defined as a decrease in SBP to <140 mmHg and/or by ≥20 mmHg and in DBP to <90 mmHg and/or by ≥10 mmHg. A second response criterion defined blood pressure reduction below 140/90 mmHg.
Results:
Blood pressure was lowered from 180.0 ± 11.7/114.7 ± 3.1 mmHg by SBP 44.4 ± 16.8 and DBP 32.0 ± 11.3 mmHg (P < 0.0001). Response was 92.4% and 64.8% achieved <140/90 mmHg. Each titration step produced a statistically significant and clinically relevant decrease in SBP and DBP, but a level below 140/90 mmHg was achieved by >50% of the patients only after the third titration step. Adverse reactions were reported by 3.8% of the patients. The disorders were in line with the known safety profile of the study drugs.
Conclusion:
A stepped treatment approach with candesartan/HCTZ combinations is effective and safe to achieve a swift blood pressure reduction in newly diagnosed, severe hypertension. The target of <140/90 mmHg was reached by >50% of the patients only after taking the full dose of candesartan 32 mg and HCTZ 25 mg.
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