Status:
COMPLETED
A Study of a Hypertensive Population Under Treatment With Micardis® and Micardis Plus® to Control the Early Morning BP Rise (SURGE II)
Lead Sponsor:
Boehringer Ingelheim
Conditions:
Hypertension
Eligibility:
All Genders
18-80 years
Brief Summary
The primary objective was to evaluate, through the use of Home blood pressure monitoring (HBPM), the degree of BP control in the early morning hours after 8 weeks of treatment in patients with essenti...
Eligibility Criteria
Inclusion
- Patients male or female between 18 and 80 years of age
- Patients with mild to moderate essential hypertension
- Patients diagnosed with hypertension that are not currently taking antihypertensive medication or previously diagnosed hypertensive patients who are uncontrolled with their current treatment
Exclusion
- Pre-menopausal women who have no birth control, who are pregnant or nursing
- Patients with advanced hepatic impairment or advanced renal impairment
- Patients with New York Heart Association (NYHA) functional class III or IV congestive heart failure (CHF), unstable angina, acute myocardial infarction, heart surgery or stroke within the previous six months
- Patients with any type of relevant arrhythmia according to the assessment of the investigator
- Patients with any valvular disease with hemodynamic repercussion
- Patients receiving chronic administration of oral anticoagulants or digoxin
- Patients with known hypersensitivity to any component in the formulation of Micardis®, Telmisartan or Micardis Plus®, Telmisartan hydrochlorothiazide
- Patients with previous history of angioedema associated with angiotensin converting enzyme (ACE) inhibitors
- Patients with severe, uncontrolled hypertension or any form of secondary hypertension
- Patients with any other clinical conditions which, in the opinion of the investigator, would not allow for the safe completion of the protocol
Key Trial Info
Start Date :
August 1 2005
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
5248 Patients enrolled
Trial Details
Trial ID
NCT02242396
Start Date
August 1 2005
Last Update
September 17 2014
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