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Completed Phase 2 Interventional

To Evaluate the Long-Term Safety of Pregabalin in Refractory Partial Epilepsy.

ClinicalTrials.gov ID: NCT00141414

Public ClinicalTrials.gov record NCT00141414. 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 23, 2026, 2:41 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

Pregabablin Open-Label, Follow-On Safety Trial In Patients With Refractory Partial Epilepsy.

Study identification

NCT ID
NCT00141414
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
82 participants

Conditions and interventions

Interventions

  • Pregabalin Drug

Drug

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
Oct 31, 1997
Primary completion
Not listed
Completion
Sep 30, 2005
Last update posted
Dec 31, 2006

1997 – 2005

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Pfizer Investigational Site Little Rock Arkansas 72205
Pfizer Investigational Site Los Angeles California 90033
Pfizer Investigational Site Stanford California 94305
Pfizer Investigational Site Miami Florida 33136
Pfizer Investigational Site Plantation Florida 33317
Pfizer Investigational Site Indianapolis Indiana 46202
Pfizer Investigational Site Indianapolis Indiana 46254
Pfizer Investigational Site Baltimore Maryland 21201
Pfizer Investigational Site Baltimore Maryland 21287
Pfizer Investigational Site Boston Massachusetts 02215
Pfizer Investigational Site Ann Arbor Michigan 48108-0768
Pfizer Investigational Site Saint Paul Minnesota 55102
Pfizer Investigational Site Chesterfield Missouri 63017
Pfizer Investigational Site New York New York 10016
Pfizer Investigational Site New York New York 10032
Pfizer Investigational Site Rochester New York 14642
Pfizer Investigational Site The Bronx New York 10467
Pfizer Investigational Site Winston-Salem North Carolina 27157
Pfizer Investigational Site Cleveland Ohio 44195
Pfizer Investigational Site Columbus Ohio 43210
Pfizer Investigational Site Philadelphia Pennsylvania 19104
Pfizer Investigational Site Nashville Tennessee 37232
Pfizer Investigational Site Madison Wisconsin 53715
Pfizer Investigational Site 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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00141414, 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 31, 2006 · Synced Jul 23, 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 NCT00141414 live on ClinicalTrials.gov.

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