Clinical trial

Prospective Randomised Investigation of the Safety and Efficacy of Micardis® vs…

NCT00274612 · Boehringer Ingelheim, Industry · Completed

Key facts

NCT number NCT00274612
Title Prospective Randomised Investigation of the Safety and Efficacy of Micardis® vs Ramipril Using ABPM
Official title A Prospective Randomised Open- Label Blinded-Endpoint (PROBE) Trial Comparing Telmisartan (MICARDIS®) (40-80-80mg QD) and Ramipril (2.5-5--10mg QD) in Patients With Mild-to-Moderate Hypertension Using Ambulatory Blood Pressure Monitoring. PRISMA = Prospective Randomised Investigation of the Safety…
Acronym PRISMA
Lead sponsor Boehringer Ingelheim, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Hypertension
Intervention type Drug
Interventions Telmisartan, Ramipril
Enrollment 801
Start date Oct 1, 2002
Primary completion Nov 1, 2003
Completion Nov 1, 2003
First posted Jan 11, 2006
Last update posted Nov 1, 2013
Countries Austria, France, Germany, Netherlands, South Africa, Spain, Switzerland, United Kingdom

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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