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Completed Phase 4 Interventional Results available

An Examination of the Blood Pressure Lowering Ability and Safety of Olmesartan Medoxomil in Patients With Type II Diabetes

ClinicalTrials.gov ID: NCT00403481

Public ClinicalTrials.gov record NCT00403481. 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 28, 2026, 2:10 PM 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, Open Label, Single Arm Study to Evaluate the Safety and Efficacy of an Olmesartan Medoxomil Based Treatment Regimen in Type II Diabetic Patients With Hypertension

Brief summary

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

This study will examine the ability of olmesartan medoxomil to lower the blood pressure of patients with Type II diabetes and high blood pressure. The medication being tested has been approved by the FDA for the treatment of high blood pressure.

Study identification

NCT ID
NCT00403481
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Daiichi Sankyo
Industry
Enrollment
192 participants

Conditions and interventions

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
Nov 2006 (Type not available)
Primary completion
Nov 2007 (Actual)
Completion
Dec 2007 (Actual)
Last update posted
Nov 3, 2016

2006 – 2007

United States locations

U.S. sites
27
U.S. states
19
U.S. cities
27
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Mesa Arizona — —
Not listed Searcy Arkansas — —
Not listed Los Angeles California — —
Not listed Roseville California — —
Not listed Tustin California — —
Not listed DeLand Florida — —
Not listed Pembroke Pines Florida — —
Not listed Chicago Illinois — —
Not listed Wichita Kansas — —
Not listed Madisonville Kentucky — —
Not listed Auburn Maine — —
Not listed Baltimore Maryland — —
Not listed Oxon Hill Maryland — —
Not listed Jackson Mississippi — —
Not listed Florissant Missouri — —
Not listed Williamsville New York — —
Not listed Charlotte North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed New Talenwell Tennessee — —
Not listed New Tazewell Tennessee — —
Not listed Colleyville Texas — —
Not listed Corpus Christi Texas — —
Not listed Richardson Texas — —
Not listed Murray Utah — —
Not listed Norfolk Virginia — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00403481, 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 Nov 3, 2016 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00403481 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →