Essential Hypertension Clinical Trial
Official title:
Monotherapy Versus Dual Therapy for Initial Treatment for Hypertension
To test whether the current custom of initiating treatment for hypertension with a single drug is less effective in the short-term than initial combination therapy, and results in the eventual need for comparatively more antihypertensive drug therapy.
To determine if patients randomised to more aggressive (combination therapy) treatment for
the initial treatment of hypertension have better blood pressure control compared to those
randomised to less aggressive (monotherapy) treatment despite subsequent add-on treatment
being similar in each group. This will test the hypothesis that monotherapy patients 'never
catch up' with combination therapy patients.
1. To determine if this 'never catch-up' phenomenon of improved BP control persists for at
least one year.
2. To understand the underlying mechanism of improved BP control; specifically:
1. To determine if it is due to haemodynamic compensation, such as increased sodium
retention and volume expansion.
2. To determine if it is due to increased peripheral resistance.
3. To understand the predictors of BP control i.e. age, baseline renin status, sodium
status and plasma volume.
4. To validate the National Institute for Clinical Excellence / British Hypertension
Society joint guideline ACD algorithm by comparing BP control in the monotherapy
crossover arm of phase 1 and to correlate this with age (≤ 55 or > 55y), and baseline
characteristics such as renin.
5. To determine the safety and tolerability of a strategy of prescribing combination
therapy as the initial step versus monotherapy as the initial step.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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