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Completed Phase 4 Interventional

PROBE Investigation of the Safety & Efficacy of Telmisartan (Micardis®) vs Ramipril (Altace®) Using ABPM in HTN

ClinicalTrials.gov ID: NCT00274599

Public ClinicalTrials.gov record NCT00274599. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 7:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Randomised, Open-Label, Blinded-Endpoint, Parallel Group, Multicentre, Forced-Titration, 14-Week Treatment Study Comparing MICARDIS® (Telmisartan 40-80-80 mg, QD) and ALTACE® (Ramipril 2.5-5-10 mg, QD) in Patients With Mild-to-Moderate Hypertension Using Ambulatory Blood Pressure Monitoring

Study identification

NCT ID
NCT00274599
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
812 participants

Conditions and interventions

Conditions

Interventions

  • Telmisartan Drug
  • Ramipril Drug

Drug

Eligibility (public fields only)

Age range
19 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 8, 2002
Primary completion
Nov 29, 2003
Completion
Not listed
Last update posted
Dec 5, 2023

Started 2002

United States locations

U.S. sites
43
U.S. states
25
U.S. cities
43
Facility City State ZIP Site status
Boehringer Ingelheim Investigational Site Birmingham Alabama
Boehringer Ingelheim Investigational Site Phoenix Arizona
Boehringer Ingelheim Investigational Site Tucson Arizona
Harold B. Betton, M.D. Little Rock Arkansas
Attn: Ginger Paselk Long Beach California
Boehringer Ingelheim Investigational Site Los Angeles California
Boehringer Ingelheim Investigational Site Orange California
Boehringer Ingelheim Investigational Site San Diego California
Boehringer Ingelheim Investigational Site Santa Ana California
Boehringer Ingelheim Investigational Site Santa Rosa California
Boehringer Ingelheim Investigational Site Vista California
Boehringer Ingelheim Investigational Site Hamden Connecticut
Boehringer Ingelheim Investigational Site Daytona Beach Florida
Boehringer Ingelheim Investigational Site Fort Lauderdale Florida
Boehringer Ingelheim Investigational Site Melbourne Florida
Boehringer Ingelheim Investigational Site Marietta Georgia
Boehringer Ingelheim Investigational Site Boise Idaho
Boehringer Ingelheim Investigational Site Meridian Idaho
Boehringer Ingelheim Investigational Site Chicago Illinois
Boehringer Ingelheim Investigational Site Orland Park Illinois
GFI Pharmaceuticals Evansville Indiana
Boehringer Ingelheim Investigational Site Newton Kansas
Boehringer Ingelheim Investigational Site Wichita Kansas
Boehringer Ingelheim Investigational Site Metairie Louisiana
Boehringer Ingelheim Investigational Site Auburn Maine
Boehringer Ingelheim Investigational Site Moorestown New Jersey
Boehringer Ingelheim Investigational Site Albuquerque New Mexico
Boehringer Ingelheim Investigational Site East Syracuse New York
Boehringer Ingelheim Investigational Site White Plains New York
Boehringer Ingelheim Investigational Site Charlotte North Carolina
Boehringer Ingelheim Investigational Site Winston-Salem North Carolina
Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma
Boehringer Ingelheim Investigational Site Portland Oregon
Boehringer Ingelheim Investigational Site Levittown Pennsylvania
Boehringer Ingelheim Investigational Site Anderson South Carolina
Spartanburg Medical Research Spartanburg South Carolina
Boehringer Ingelheim Investigational Site Dallas Texas
R/D Clinical Research, Inc. Lake Jackson Texas
Boehringer Ingelheim Investigational Site Salt Lake City Utah
Boehringer Ingelheim Investigational Site Lacey Washington
Boehringer Ingelheim Investigational Site Lakewood Washington
Boehringer Ingelheim Investigational Site Tacoma Washington
Boehringer Ingelheim Investigational Site Charleston West Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 31 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00274599, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 5, 2023 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00274599 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →