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Safety and Efficacy Evaluation Of Pregabalin (Lyrica) With Patients With Generalized Anxiety Disorder
This study is currently recruiting participants.
Verified by Pfizer, November 2009
First Received: February 15, 2008   Last Updated: November 19, 2009   History of Changes
Sponsor: Pfizer
Information provided by: Pfizer
ClinicalTrials.gov Identifier: NCT00624780
  Purpose

The purpose of this study is to characterize the safety and efficacy in patients with generalized anxiety disorder after short- (3 months) and long-term (6 months) use of Pregabalin (Lyrica).


Condition Intervention Phase
Generalized Anxiety Disorder
Drug: Pregabalin
Drug: Lorazepam
Drug: Placebo
Phase IV

Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Investigator), Parallel Assignment, Safety/Efficacy Study
Official Title: Long Term Safety And Efficacy Study Of Pregabalin (Lyrica) In Subjects With Generalized Anxiety Disorder

Resource links provided by NLM:


Further study details as provided by Pfizer:

Primary Outcome Measures:
  • Safety endpoints: Adverse events at 3 and 6 months, Physicians Withdrawal Checklist (PWC), Rebound Anxiety (HAM-A), Discontinuation Emergent Signs and Symptoms (DESS) [ Time Frame: 3 and 6 months ] [ Designated as safety issue: Yes ]
  • Efficacy endpoints: Hamilton Anxiety Scale (HAM-A), Clinical Global Impression-Severity (CGI-S), Clinical Global Impression-Improvement (CGI-I). [ Time Frame: 3 and 6 months ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Adverse events [ Time Frame: through study ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 600
Study Start Date: April 2009
Estimated Study Completion Date: June 2011
Estimated Primary Completion Date: May 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental Drug: Pregabalin
Pregabalin 150-300 mg given twice a day
2: Active Comparator Drug: Lorazepam
Lorazepam 3-4 mg given twice a day
3: Experimental Drug: Pregabalin
Pregabalin 450-600 mg given twice a day
4: Placebo Comparator Drug: Placebo
Placebo

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Diagnosis of GAD. HAM-A score >=18 and HAM-D (item 1) score >=2 at screening and baseline. Needs pharmacological treatment.

Exclusion Criteria:

Current or past diagnosis of any other DSM IV Axis I disorders. A history of failed treatment with a benzodiazepine. Any clinically significant, serious, or unstable hematologic, autoimmune, endocrine, cardiovascular, renal, hepatic, gastrointestinal, or neurological disorder.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00624780

Contacts
Contact: Pfizer CT.gov Call Center 1-800-718-1021

  Hide Study Locations
Locations
Argentina
Pfizer Investigational Site Recruiting
Buenos Aires, Argentina, C1405BOA
Pfizer Investigational Site Not yet recruiting
Buenos Aires, Argentina, C1428AQK
Pfizer Investigational Site Recruiting
Buenos Aires, Argentina, C1115AAJ
Argentina, Buenos Aires
Pfizer Investigational Site Recruiting
La Plata, Buenos Aires, Argentina, B1904ADM
Argentina, Prov. de Buenos Aires
Pfizer Investigational Site Recruiting
Lanus, Prov. de Buenos Aires, Argentina, B1824IBR
Austria
Pfizer Investigational Site Recruiting
Wien, Austria, A-1090
Pfizer Investigational Site Recruiting
Wien, Austria, A-1010
Czech Republic
Pfizer Investigational Site Recruiting
Praha 10- Strasnice, Czech Republic, 10000
Pfizer Investigational Site Recruiting
Praha 6, Czech Republic, 160 00
Pfizer Investigational Site Recruiting
Brno, Czech Republic, 602 00
Pfizer Investigational Site Recruiting
Litomerice, Czech Republic, 412 01
Pfizer Investigational Site Not yet recruiting
Melnik, Czech Republic, 276 01
Pfizer Investigational Site Recruiting
Strakonice, Czech Republic, 386 01
Pfizer Investigational Site Not yet recruiting
Ceske Budejovice, Czech Republic, 370 87
Czech Republic, 387 42
Pfizer Investigational Site Recruiting
Lnare, 387 42, Czech Republic
Finland
Pfizer Investigational Site Recruiting
Turku, Finland, 20100
Pfizer Investigational Site Recruiting
Seinajoki, Finland, 60100
Pfizer Investigational Site Recruiting
Hus, Finland, 00029
Pfizer Investigational Site Recruiting
Kuopio, Finland, 70110
Pfizer Investigational Site Recruiting
Joensuu, Finland, 80100
Greece
Pfizer Investigational Site Not yet recruiting
Ioannina, Greece, 45600
Pfizer Investigational Site Not yet recruiting
Thessaloniki, Greece, 54636
Pfizer Investigational Site Not yet recruiting
Athens, Greece, 11528
Pfizer Investigational Site Not yet recruiting
Thessaloniki, Greece, 56429
India, Ahmedabad
Pfizer Investigational Site Not yet recruiting
Ellisbridge, Ahmedabad, India, 380 006
India, Andhra Pradesh
Pfizer Investigational Site Not yet recruiting
Tirupati, Andhra Pradesh, India, 517 507
India, Karnataka
Pfizer Investigational Site Recruiting
Mangalore, Karnataka, India, 575001
India, Maharashtra
Pfizer Investigational Site Not yet recruiting
Pune, Maharashtra, India, 411 030
India, Tamil Nadu
Pfizer Investigational Site Recruiting
Chennai, Tamil Nadu, India, 600 003
Indonesia
Pfizer Investigational Site Recruiting
Surabaya, Indonesia
Pfizer Investigational Site Recruiting
Yogyakarta, Indonesia
Pfizer Investigational Site Recruiting
Surabaya, East Java, Indonesia
Indonesia, Bali
Pfizer Investigational Site Recruiting
Denpasar, Bali, Indonesia
Indonesia, Jakarta
Pfizer Investigational Site Recruiting
Jakarta Selatan, Jakarta, Indonesia, 10430
Indonesia, Jakarta Selatan
Pfizer Investigational Site Recruiting
Jakarta, Jakarta Selatan, Indonesia
Lithuania
Pfizer Investigational Site Recruiting
Kaunas, Lithuania, 50185
Pfizer Investigational Site Recruiting
Kaunas, Lithuania, 50425
Pfizer Investigational Site Recruiting
Klaipeda, Lithuania, 94231
Pfizer Investigational Site Recruiting
Vilnius, Lithuania, 09112
Russian Federation
Pfizer Investigational Site Not yet recruiting
St. Petersburg, Russian Federation, 192019
Serbia
Pfizer Investigational Site Recruiting
Belgrade, Serbia, 11000
Slovenia
Pfizer Investigational Site Recruiting
Ljubljana, Slovenia
Spain
Pfizer Investigational Site Recruiting
Zamora, Spain, 49021
Spain, ASTURIAS
Pfizer Investigational Site Recruiting
Langreo, ASTURIAS, Spain, 33900
Spain, BARCELONA
Pfizer Investigational Site Not yet recruiting
Sabadell, BARCELONA, Spain, 08208
Spain, CADIZ
Pfizer Investigational Site Not yet recruiting
Jerez de La Frontera, CADIZ, Spain, 11407
Turkey
Pfizer Investigational Site Recruiting
Istanbul, Turkey, 34203
Pfizer Investigational Site Not yet recruiting
Izmir, Turkey, 35340
Pfizer Investigational Site Not yet recruiting
Manisa, Turkey, 45020
Pfizer Investigational Site Recruiting
Kocaeli, Turkey, 41380
Sponsors and Collaborators
Pfizer
Investigators
Study Director: Pfizer CT.gov Call Center Pfizer
  More Information

Additional Information:
No publications provided

Responsible Party: Pfizer, Inc. ( Director, Clinical Trials Disclosure Group )
Study ID Numbers: A0081147
Study First Received: February 15, 2008
Last Updated: November 19, 2009
ClinicalTrials.gov Identifier: NCT00624780     History of Changes
Health Authority: Finland: National Agency of Medicines (Lääkelaitos)

Additional relevant MeSH terms:
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
GABA Modulators
Physiological Effects of Drugs
Psychotropic Drugs
Antiemetics
Lorazepam
Pathologic Processes
Sensory System Agents
Mental Disorders
Therapeutic Uses
Hypnotics and Sedatives
Analgesics
Disease
Tranquilizing Agents
Gastrointestinal Agents
Central Nervous System Depressants
Pregabalin
Pharmacologic Actions
Anxiety Disorders
Autonomic Agents
GABA Agents
Anti-Anxiety Agents
Peripheral Nervous System Agents
Central Nervous System Agents
Anticonvulsants

ClinicalTrials.gov processed this record on November 27, 2009