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Completed Phase 2 Interventional Results available

PK/PD, Long-term Safety and Efficacy of Tamsulosin Treatment in Children With Neurogenic Bladder

ClinicalTrials.gov ID: NCT00340704

Public ClinicalTrials.gov record NCT00340704. 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 21, 2026, 6:04 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

An Uncontrolled, Open-label, Titration, Long-term Safety (up to 12 Months) and Efficacy Study of Tamsulosin Hydrochloride in Children With Neuropathic Bladder, With a Randomized Pharmacokinetic Sub-study Investigating Low, Medium and High Dose Ranges.

Study identification

NCT ID
NCT00340704
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
143 participants

Conditions and interventions

Interventions

  • tamsulosin hydrochloride Drug

Drug

Eligibility (public fields only)

Age range
2 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
Mar 31, 2006
Primary completion
May 31, 2009
Completion
May 31, 2009
Last update posted
Feb 16, 2016

2006 – 2009

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Not listed Birmingham Alabama 35233
Not listed Los Angeles California 90027
Not listed Jacksonville Florida 32207
Not listed Tampa Florida 33614
Not listed Springfield Illinois 62702
Not listed Indianapolis Indiana 46202
Not listed Shreveport Louisiana 71106
Not listed St Louis Missouri 63110
Not listed Buffalo New York 14222
Not listed Lake Success New York 11042
Not listed Tarrytown New York 10591
Not listed Winston-Salem North Carolina 27157
Not listed Akron Ohio 44308
Not listed Oklahoma City Oklahoma 73104
Not listed Nashville Tennessee 37232
Not listed Dallas Texas 75235
Not listed Houston Texas 77030
Not listed Salt Lake City Utah 84132
Not listed Madison Wisconsin 53792

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 53 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00340704, 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 Feb 16, 2016 · Synced Jul 21, 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 NCT00340704 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →