Evaluation of Long-Term Safety and Efficacy of Pregabalin in Patients With Partial Seizures.

NCT ID: NCT00150293

Last Updated: 2015-03-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

337 participants

Study Classification

INTERVENTIONAL

Study Start Date

2002-03-31

Study Completion Date

2005-11-30

Brief Summary

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To determine long-term safety and efficacy of pregabalin in patients with partial seizures.

Detailed Description

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Conditions

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Seizure Disorder, Partial

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Pregabalin

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Have received double-blind study medication and wish to receive open-label pregabalin.

Exclusion Criteria

* Cannot be pregnant or considering becoming pregnant during the course of the study.
* Cannot be receiving any concomitant medication that could alter the effectiveness of the pregabalin response or affect seizure frequency.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Deakin, Australian Capital Territory, Australia

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Camperdown, New South Wales, Australia

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Chastwood, New South Wales, Australia

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Cairns, Queensland, Australia

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Maroochydore, Queensland, Australia

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Footscray, Victoria, Australia

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Parkville, Victoria, Australia

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Perth, Western Australia, Australia

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Auenbruggerplatz 22, , Austria

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Graz, , Austria

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Innsbruck, , Austria

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Linz, , Austria

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Vienna, , Austria

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Leuven, , Belgium

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Calgary, Alberta, Canada

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Edmonton, Alberta, Canada

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Penticton, British Columbia, Canada

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Vancouver, British Columbia, Canada

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Halifax, Nova Scotia, Canada

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Barrie, Ontario, Canada

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London, Ontario, Canada

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Ottawa, Ontario, Canada

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Toronto, Ontario, Canada

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Windsor, Ontario, Canada

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Montreal, Quebec, Canada

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Montreal, Quebec, Canada

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Montreal, Quebec, Canada

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Québec, Quebec, Canada

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Regina, Saskatchewan, Canada

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Saskatoon, Saskatchewan, Canada

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Ulm, Baden-Wurttemberg, Germany

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Berlin, , Germany

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Bernau, , Germany

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Bonn, , Germany

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Dresden, , Germany

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Erlangen, , Germany

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Essen, , Germany

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Frankfurt, , Germany

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Freiburg im Breisgau, , Germany

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Göttingen, , Germany

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Hamburg, , Germany

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Mainz, , Germany

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München, , Germany

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AE Breda, , Netherlands

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Blaricum, , Netherlands

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Ve Heeze, , Netherlands

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Bialystok, , Poland

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Bydgoszcz, , Poland

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Choroszcz, , Poland

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Gdansk, , Poland

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Gdansk, , Poland

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Grudziądz, , Poland

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Katowice, , Poland

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Krakow, , Poland

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Lublin, , Poland

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Mosina, , Poland

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Olsztyn, , Poland

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Poznan, , Poland

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Poznan, , Poland

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Płock, , Poland

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Torun, , Poland

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Warsaw, , Poland

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Warsaw, , Poland

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Warsaw, , Poland

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Coimbra, , Portugal

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Porto, , Portugal

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Barcelona, Barcelona, Spain

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Granada, Granada, Spain

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Málaga, Malaga, Spain

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Zaragoza, Zaragoza, Spain

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Girona, , Spain

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Madrid, , Spain

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Madrid, , Spain

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Middlesbrough, N. York, United Kingdom

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Washington, Tyne & Wear, United Kingdom

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Blackpool, , United Kingdom

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Dundee, , United Kingdom

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Glasgow, , United Kingdom

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Leeds, , United Kingdom

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London, , United Kingdom

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Northampton, , United Kingdom

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Wolverhampton, , United Kingdom

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Countries

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Australia Austria Belgium Canada Germany Netherlands Poland Portugal Spain United Kingdom

Other Identifiers

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1008-114

Identifier Type: -

Identifier Source: org_study_id

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