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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