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Completed Phase 2 Interventional Results available

Pramipexole Pilot Phase II Study in Children and Adolescents With Tourette Disorder According to DSM-IV Criteria

ClinicalTrials.gov ID: NCT00558467

Public ClinicalTrials.gov record NCT00558467. 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 Jul 22, 2026, 10:37 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 Randomized, Double-blind, Placebo-controlled, Flexible Dose Study to Evaluate Efficacy and Safety of Pramipexole Immediate Release (0.125-0.5mg/Day) Versus Placebo for 6 Weeks in Children and Adolescents (Age 6-17 Inclusive) Diagnosed With Tourette Disorder According to DSM IV Criteria.

Study identification

NCT ID
NCT00558467
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
63 participants

Conditions and interventions

Interventions

  • pramipexole immediate release (IR) Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
6 Years to 17 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
Dec 31, 2007
Primary completion
May 31, 2009
Completion
Not listed
Last update posted
May 15, 2014

Started 2008

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
248.644.0026 Boehringer Ingelheim Investigational Site Bradenton Florida
248.644.0025 Boehringer Ingelheim Investigational Site Tampa Florida
248.644.0006 Boehringer Ingelheim Investigational Site Columbus Georgia
248.644.0012 Boehringer Ingelheim Investigational Site Chicago Illinois
248.644.0005 Boehringer Ingelheim Investigational Site Cambridge Massachusetts
248.644.0003 Boehringer Ingelheim Investigational Site Manhasset New York
248.644.0009 Boehringer Ingelheim Investigational Site New York New York
248.644.0018 Boehringer Ingelheim Investigational Site New York New York
248.644.0013 Boehringer Ingelheim Investigational Site Orangeburg New York
248.644.0029 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma
248.644.0010 Boehringer Ingelheim Investigational Site Providence Rhode Island
248.644.0030 Boehringer Ingelheim Investigational Site Memphis Tennessee
248.644.0008 Boehringer Ingelheim Investigational Site Houston Texas
248.644.0023 Boehringer Ingelheim Investigational Site 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00558467, 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 May 15, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00558467 live on ClinicalTrials.gov.

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