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Completed Phase 4 Interventional Results available

Effectiveness and Safety of Ramipril Alone Compared With Telmisartan Alone and in Combination With Ramipril in Patients at High Risk for Cardiovascular Events. Patients Intolerant to Ramipril Were Entered in TRANSCEND, Telmisartan Compared to Placebo.

ClinicalTrials.gov ID: NCT00153101

Public ClinicalTrials.gov record NCT00153101. 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 Oct 30, 2026, 4:44 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

ONTARGET ONgoing Telmisartan Alone and in Combination With Ramipril Global Endpoint Trial A Large, Simple Randomized Trial of an Angiotensin II Receptor Antagonist (Telmisartan) and an ACE-Inhibitor (Ramipril) in Patients at High Risk for Cardiovascular Events and TRANSCEND Telmisartan Randomized AssessmeNt Study in aCE iNtolerant Subjects With Cardiovascular Disease. A Parallel Study Comparing the Effects of Telmisartan With Placebo and Outcomes in Patients at High Risk for Cardiovascular Events and Intolerant to ACE-I.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The Ongoing Telmisartan Alone and in combination wiht Ramipril Global Endpoint trial (ONTARGET): The primary objectives are to determine if (a) telmisartan 80mg daily and ramipril 10mg daily combination therapy is more effective in reducing the composite endpoint of Cardiovascular Death (CV) death, Myocardial infarction (MI), stroke or hospitalization for Congestive Heart Failure (CHF) compared with ramipril 10mg alone; and (b) telmisartan 80mg daily is at least as effective as (i.e. not less effective than) ramipril 10mg daily, on this endpoint. Telmisartan Randomised Assessment Study in Angiotension converting Enzyme inhibitor intolerant subjects with Cardiovascular Disease. (TRANSCEND): The primary objective of the study is to determine if treatment with telmisartan 80mg daily is superior to placebo reducing the composite endpoint of Cardiovascular Death (CV), Myocardial Infarction ( MI)I, stroke or hospitalization for Congestive Heart Failure (CHF) in patients who are intolerant to Angiotension Converting Enzyme inhibitors.

Study identification

NCT ID
NCT00153101
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
31,546 participants

Conditions and interventions

Eligibility (public fields only)

Age range
55 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
Nov 2001 (Type not available)
Primary completion
Jun 2008 (Actual)
Completion
Not listed
Last update posted
May 20, 2014

Started 2001

United States locations

U.S. sites
100
U.S. states
33
U.S. cities
87
Facility City State ZIP Site status
502.373.0256 Boehringer Ingelheim Investigational Site Athens Alabama — —
502.373.0251 Boehringer Ingelheim Investigational Site Birmingham Alabama — —
502.373.0182 Boehringer Ingelheim Investigational Site Phoenix Arizona — —
502.373.0188 Boehringer Ingelheim Investigational Site Phoenix Arizona — —
502.373.0189 Boehringer Ingelheim Investigational Site Tucson Arizona — —
502.373.0177 Boehringer Ingelheim Investigational Site Tuscon Arizona — —
502.373.0209 Boehringer Ingelheim Investigational Site Bentonville Arkansas — —
502.373.0173 Boehringer Ingelheim Investigational Site Concord California — —
502.373.0266 Boehringer Ingelheim Investigational Site Harbor City California — —
502.373.0283 Boehringer Ingelheim Investigational Site Loma Linda California — —
502.373.0180 Boehringer Ingelheim Investigational Site Los Angeles California — —
502.373.0175 Boehringer Ingelheim Investigational Site Sacramento California — —
502.373.0165 Boehringer Ingelheim Investigational Site San Diego California — —
502.373.0228 Boehringer Ingelheim Investigational Site San Leandro California — —
502.373.0205 Boehringer Ingelheim Investigational Site Sylmar California — —
502.373.0277 Boehringer Ingelheim Investigational Site West Hills California — —
502.373.0226 Boehringer Ingelheim Investigational Site Bridgeport Connecticut — —
502.373.0174 Boehringer Ingelheim Investigational Site Farmington Connecticut — —
502.373.0258 Boehringer Ingelheim Investigational Site Washington D.C. District of Columbia — —
502.373.0179 Boehringer Ingelheim Investigational Site Gainesville Florida — —
502.373.0183 Boehringer Ingelheim Investigational Site Palm Harbor Florida — —
502.373.0240 Boehringer Ingelheim Investigational Site Panama City Florida — —
502.373.0171 Boehringer Ingelheim Investigational Site Tampa Florida — —
502.373.0282 Boehringer Ingelheim Investigational Site Vero Beach Florida — —
502.373.0214 Boehringer Ingelheim Investigational Site Weston Florida — —
502.373.0161 Boehringer Ingelheim Investigational Site Augusta Georgia — —
502.373.0193 Boehringer Ingelheim Investigational Site Augusta Georgia — —
502.373.0201 Boehringer Ingelheim Investigational Site Augusta Georgia — —
502.373.0223 Boehringer Ingelheim Investigational Site Conyers Georgia — —
502.373.0268 Boehringer Ingelheim Investigational Site Sandersville Georgia — —
502.373.0245 Boehringer Ingelheim Investigational Site Savannah Georgia — —
502.373.0199 Boehringer Ingelheim Investigational Site Tucker Georgia — —
502.373.0162 Boehringer Ingelheim Investigational Site Valdosta Georgia — —
502.373.0203 Boehringer Ingelheim Investigational Site Pocatello Idaho — —
502.373.0244 Boehringer Ingelheim Investigational Site Burbank Illinois — —
502.373.0272 Boehringer Ingelheim Investigational Site Chicago Illinois — —
502.373.0217 Boehringer Ingelheim Investigational Site Olympia Fields Illinois — —
502.373.0270 Boehringer Ingelheim Investigational Site Des Moines Iowa — —
502.373.0167 Boehringer Ingelheim Investigational Site Monroe Louisiana — —
502.373.0158 Boehringer Ingelheim Investigational Site Shreveport Louisiana — —
502.373.0247 Boehringer Ingelheim Investigational Site Baltimore Maryland — —
502.373.0284 Boehringer Ingelheim Investigational Site Boston Massachusetts — —
502.373.0229 Boehringer Ingelheim Investigational Site Springfield Massachusetts — —
502.373.0237 Boehringer Ingelheim Investigational Site Wyandotte Michigan — —
502.373.0208 Boehringer Ingelheim Investigational Site Minneapolis Minnesota — —
502.373.0232 Boehringer Ingelheim Investigational Site Minneapolis Minnesota — —
502.373.0231 Boehringer Ingelheim Investigational Site Saint Paul Minnesota — —
502.373.0181 Boehringer Ingelheim Investigational Site Biloxi Mississippi — —
502.373.0185 Boehringer Ingelheim Investigational Site Cleveland Mississippi — —
502.373.0254 Boehringer Ingelheim Investigational Site Jackson Mississippi — —
502.373.0195 Boehringer Ingelheim Investigational Site Kansas City Missouri — —
502.373.0207 Boehringer Ingelheim Investigational Site St Louis Missouri — —
502.373.0239 Boehringer Ingelheim Investigational Site St Louis Missouri — —
502.373.0279 Boehringer Ingelheim Investigational Site Omaha Nebraska — —
502.373.0169 Boehringer Ingelheim Investigational Site North Las Vegas Nevada — —
502.373.0157 Boehringer Ingelheim Investigational Site Camden New Jersey — —
502.373.0202 Boehringer Ingelheim Investigational Site East Orange New Jersey — —
502.373.0191 Boehringer Ingelheim Investigational Site Newark New Jersey — —
502.373.0271 Boehringer Ingelheim Investigational Site Westwood New Jersey — —
502.373.0213 Boehringer Ingelheim Investigational Site Brooklyn New York — —
502.373.0230 Boehringer Ingelheim Investigational Site Buffalo New York — —
502.373.0288 Boehringer Ingelheim Investigational Site Kingston New York — —
502.373.0238 Boehringer Ingelheim Investigational Site New York New York — —
502.373.0252 Boehringer Ingelheim Investigational Site New York New York — —
502.373.0286 Boehringer Ingelheim Investigational Site New York New York — —
502.373.0166 Boehringer Ingelheim Investigational Site Northport New York — —
502.373.0156 Boehringer Ingelheim Investigational Site Rochester New York — —
502.373.0264 Boehringer Ingelheim Investigational Site Rochester New York — —
502.373.0227 Boehringer Ingelheim Investigational Site Scarsdale New York — —
502.373.0150 Boehringer Ingelheim Investigational Site The Bronx New York — —
502.373.0163 Boehringer Ingelheim Investigational Site Westfield New York — —
502.373.0241 Boehringer Ingelheim Investigational Site Williamsville New York — —
502.373.0273 Boehringer Ingelheim Investigational Site Durham North Carolina — —
502.373.0261 Boehringer Ingelheim Investigational Site Winston-Salem North Carolina — —
502.373.0222 Boehringer Ingelheim Investigational Site Fargo North Dakota — —
502.373.0155 Boehringer Ingelheim Investigational Site Cincinnati Ohio — —
502.373.0164 Boehringer Ingelheim Investigational Site Cleveland Ohio — —
502.373.0168 Boehringer Ingelheim Investigational Site Dayton Ohio — —
502.373.0159 Boehringer Ingelheim Investigational Site Mansfield Ohio — —
502.373.0178 Boehringer Ingelheim Investigational Site Oklahoma City Ohio — —
502.373.0259 Boehringer Ingelheim Investigational Site Guthrie Oklahoma — —
502.373.0154 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma — —
502.373.0152 Boehringer Ingelheim Investigational Site Tulsa Oklahoma — —
502.373.0243 Boehringer Ingelheim Investigational Site Portland Oregon — —
502.373.0265 Boehringer Ingelheim Investigational Site Erie Pennsylvania — —
502.373.0153 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania — —
502.373.0274 Boehringer Ingelheim Investigational Site Sellersville Pennsylvania — —
502.373.0184 Boehringer Ingelheim Investigational Site Charleston South Carolina — —
502.373.0248 Boehringer Ingelheim Investigational Site Columbia South Carolina — —
502.373.0172 Boehringer Ingelheim Investigational Site Dallas Texas — —
502.373.0187 Boehringer Ingelheim Investigational Site Dallas Texas — —
502.373.0219 Boehringer Ingelheim Investigational Site Dallas Texas — —
502.373.0275 Boehringer Ingelheim Investigational Site Dallas Texas — —
502.373.0221 Boehringer Ingelheim Investigational Site Fort Worth Texas — —
502.373.0206 Boehringer Ingelheim Investigational Site Houston Texas — —
502.373.0234 Boehringer Ingelheim Investigational Site Houston Texas — —
502.373.0280 Boehringer Ingelheim Investigational Site Houston Texas — —
502.373.0249 Boehringer Ingelheim Investigational Site Burke Virginia — —
502.373.0281 Boehringer Ingelheim Investigational Site Seattle Washington — —
502.373.0212 Boehringer Ingelheim Investigational Site Milwaukee Wisconsin — —

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 632 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00153101, 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 May 20, 2014 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00153101 live on ClinicalTrials.gov.

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