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Completed Phase 3 Interventional Results available

Telmisartan Fixed Dose Combination vs Amlodipine in Hypertensive Patients With Type 2 Diabetes Mellitus

ClinicalTrials.gov ID: NCT00877929

Public ClinicalTrials.gov record NCT00877929. 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 May 6, 2026, 8:16 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

An 8-week Randomised, Double-blind Study to Compare the Fixed-dose Combination of Telmisartan 80 + Amlodipine 10mg Versus Amlodipine 10 mg Monotherapy as First Line Therapy in Type 2 Diabetes Patients With Hypertension.

Study identification

NCT ID
NCT00877929
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
706 participants

Conditions and interventions

Conditions

Interventions

  • Amlodipine 10 Drug
  • Telmisartan 80 Drug

Drug

Eligibility (public fields only)

Age range
18 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
Jan 31, 2009
Primary completion
Apr 30, 2010
Completion
Not listed
Last update posted
Mar 11, 2014

Started 2009

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
1235.21.901 Boehringer Ingelheim Investigational Site Long Beach California
1235.21.907 Boehringer Ingelheim Investigational Site Tustin California
1235.21.913 Boehringer Ingelheim Investigational Site Fort Lauderdale Florida
1235.21.910 Boehringer Ingelheim Investigational Site Hollywood Florida
1235.21.903 Boehringer Ingelheim Investigational Site Pembroke Pines Florida
1235.21.905 Boehringer Ingelheim Investigational Site Tucker Georgia
1235.21.916 Boehringer Ingelheim Investigational Site Olive Branch Mississippi
1235.21.915 Boehringer Ingelheim Investigational Site Hickory North Carolina
1235.21.906 Boehringer Ingelheim Investigational Site Winston-Salem North Carolina
1235.21.902 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma
1235.21.904 Boehringer Ingelheim Investigational Site Penndel Pennsylvania
1235.21.908 Boehringer Ingelheim Investigational Site Carrollton Texas
1235.21.909 Boehringer Ingelheim Investigational Site Dallas Texas
1235.21.912 Boehringer Ingelheim Investigational Site Killeen Texas
1235.21.911 Boehringer Ingelheim Investigational Site Ettrick 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 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00877929, 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 Mar 11, 2014 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00877929 live on ClinicalTrials.gov.

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