ClinicalTrials.gov record
Completed Phase 4 Interventional Results available

Telmisartan 80mg Plus Hydrochlorothiazide 25mg First Line in Moderate or Severe Hypertension

ClinicalTrials.gov ID: NCT00926289

Public ClinicalTrials.gov record NCT00926289. 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 5, 2026, 6:50 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 Randomised, Double-blind, Double Dummy, Active Controlled, Parallel Group, Forced Titration Study to Compare the Fixed-dose Combination of Telmisartan 80mg Plus Hydrochlorothiazide 25mg (T80/HCTZ25) Versus Telmisartan 80mg (T80) Monotherapy as First Line Therapy in Patients With Grade 2 or Grade 3 Hypertension (Systolic Blood Pressure (SBP) >=160 mmHg and Diastolic Blood Pressure (DBP) >=100 mmHg)

Study identification

NCT ID
NCT00926289
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
894 participants

Conditions and interventions

Conditions

Interventions

  • Hydrochlorothiazide Drug
  • Telmisartan 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
May 31, 2009
Primary completion
Mar 31, 2010
Completion
Not listed
Last update posted
Jun 26, 2014

Started 2009

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
502.550.01008 Boehringer Ingelheim Investigational Site Athens Alabama
502.550.01019 Boehringer Ingelheim Investigational Site Mobile Alabama
502.550.01015 Boehringer Ingelheim Investigational Site Lomita California
502.550.01003 Boehringer Ingelheim Investigational Site Colorado Springs Colorado
502.550.01014 Boehringer Ingelheim Investigational Site Fort Lauderdale Florida
502.550.01002 Boehringer Ingelheim Investigational Site Louisville Kentucky
502.550.01011 Boehringer Ingelheim Investigational Site New Iberia Louisiana
502.550.01009 Boehringer Ingelheim Investigational Site New Orleans Louisiana
502.550.01018 Boehringer Ingelheim Investigational Site Olive Branch Mississippi
502.550.01006 Boehringer Ingelheim Investigational Site St Louis Missouri
502.550.01016 Boehringer Ingelheim Investigational Site Charlotte North Carolina
502.550.01007 Boehringer Ingelheim Investigational Site Greensboro North Carolina
502.550.01005 Boehringer Ingelheim Investigational Site Cincinnati Ohio
502.550.01001 Boehringer Ingelheim Investigational Site Cleveland Ohio
502.550.01017 Boehringer Ingelheim Investigational Site Houston Texas
502.550.01020 Boehringer Ingelheim Investigational Site Houston Texas
502.550.01012 Boehringer Ingelheim Investigational Site San Antonio Texas
502.550.01004 Boehringer Ingelheim Investigational Site Arlington 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 88 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00926289, 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 Jun 26, 2014 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00926289 live on ClinicalTrials.gov.

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