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Completed Phase 4 Interventional Results available

A Study of the Blood Pressure Lowering Ability and Safety of Olmesartan Medoxomil in Stage I and Stage II Hypertension

ClinicalTrials.gov ID: NCT00430638

Public ClinicalTrials.gov record NCT00430638. 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 23, 2026, 12:14 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 Double-Blind, Randomized, Placebo Controlled, Parallel Group Study to Compare the Safety and Efficacy of an Olmesartan Medoxomil Based Treatment Regimen to Placebo in Patients With Stage I and Stage II Hypertension

Brief summary

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

This 16 week study will examine the ability of olmesartan medoxomil to lower the blood pressure of patients with moderate to severe high blood pressure in comparison to placebo. The medication being tested has been approved by the FDA for the treatment of high blood pressure.

Study identification

NCT ID
NCT00430638
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Daiichi Sankyo
Industry
Enrollment
278 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
Dec 2006 (Type not available)
Primary completion
Oct 2007 (Actual)
Completion
Oct 2007 (Actual)
Last update posted
Oct 2, 2018

2006 – 2007

United States locations

U.S. sites
29
U.S. states
18
U.S. cities
29
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Mobile Alabama — —
Not listed Muscle Shoals Alabama — —
Not listed Searcy Arkansas — —
Not listed Carmichael California — —
Not listed Spring Valley California — —
Not listed Coral Gables Florida — —
Not listed Deerfield Beach Florida — —
Not listed DeLand Florida — —
Not listed Fort Lauderdale Florida — —
Not listed Hialeah Florida — —
Not listed Hollywood Florida — —
Not listed Pembroke Pines Florida — —
Not listed Chicago Illinois — —
Not listed Elizabeth New Jersey — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Oklahoma City Oklahoma — —
Not listed Eugene Oregon — —
Not listed Downingtown Pennsylvania — —
Not listed Charleston South Carolina — —
Not listed Nashville Tennessee — —
Not listed New Tazewell Tennessee — —
Not listed Colleyville Texas — —
Not listed San Antonio Texas — —
Not listed Murray Utah — —
Not listed Manassas Virginia — —
Not listed Olympia Washington — —
Not listed Madison Wisconsin — —

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 NCT00430638, 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 Oct 2, 2018 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00430638 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →