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Completed Phase 3 Interventional

A Study to Evaluate the Efficacy and Safety of Eplerenone in the Treatment of Hypertension in Children.

ClinicalTrials.gov ID: NCT00147589

Public ClinicalTrials.gov record NCT00147589. 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 16, 2026, 6:31 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

Peds I (Pediatric Eplerenone Development Study I): A Randomized, Double-Blind, Placebo Withdrawal, Parallel Group, Dose-Response Study To Evaluate The Efficacy And Safety Of Eplerenone In The Treatment Of Hypertension In Children

Study identification

NCT ID
NCT00147589
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Industry
Enrollment
320 participants

Conditions and interventions

Conditions

Interventions

  • Eplerenone Drug

Drug

Eligibility (public fields only)

Age range
6 Years to 16 Years
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
Aug 31, 2004
Primary completion
Not listed
Completion
Dec 31, 2006
Last update posted
Dec 21, 2020

2004 – 2007

United States locations

U.S. sites
28
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
Pfizer Investigational Site Little Rock Arkansas
Pfizer Investigational Site Beverly Hills California
Pfizer Investigational Site Inglewood California
Pfizer Investigational Site Los Angeles California
Pfizer Investigational Site Jacksonville Florida
Pfizer Investigational Site Miami Florida
Pfizer Investigational Site Augusta Georgia
Pfizer Investigational Site Park Ridge Illinois
Pfizer Investigational Site Louisville Kentucky
Pfizer Investigational Site Shreveport Louisiana
Pfizer Investigational Site Boston Massachusetts
Pfizer Investigational Site Ann Arbor Michigan
Pfizer Investigational Site Jackson Mississippi
Pfizer Investigational Site Tupelo Mississippi
Pfizer Investigational Site Livingston New Jersey
Pfizer Investigational Site Carrboro North Carolina
Pfizer Investigational Site Chapel Hill North Carolina
Pfizer Investigational Site Pittsboro North Carolina
Pfizer Investigational Site Cleveland Ohio
Pfizer Investigational Site Columbus Ohio
Pfizer Investigational Site Youngstown Ohio
Pfizer Investigational Site Tulsa Oklahoma
Pfizer Investigational Site Portland Oregon
Pfizer Investigational Site Philadelphia Pennsylvania
Pfizer Investigational Site Memphis Tennessee
Pfizer Investigational Site Beaumont Texas
Pfizer Investigational Site Houston Texas
Pfizer Investigational Site Katy Texas

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 13 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00147589, 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 Dec 21, 2020 · Synced May 16, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00147589 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →