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Completed Phase 2 Interventional Results available

Dose-Tolerability Titration Study to Evaluate The Efficacy And Safety Of Perampanel (E2007) In Patients With Post-Herpetic Neuralgia (PHN)

ClinicalTrials.gov ID: NCT00592774

Public ClinicalTrials.gov record NCT00592774. 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, 7:22 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Tolerability Titration Study To Evaluate The Efficacy And Safety Of Perampanel (E2007) In Patients With Post-Herpetic Neuralgia (PHN)

Study identification

NCT ID
NCT00592774
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eisai Inc.
Industry
Enrollment
146 participants

Conditions and interventions

Conditions

Interventions

  • E2007 (perampanel) Drug
  • Placebo 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
Dec 31, 2007
Primary completion
Nov 30, 2008
Completion
Feb 28, 2009
Last update posted
Feb 14, 2013

2008 – 2009

United States locations

U.S. sites
42
U.S. states
18
U.S. cities
41
Facility City State ZIP Site status
Not listed Peoria Arizona
Not listed Tucson Arizona
Not listed Little Rock Arkansas
Not listed Los Angeles California
Not listed Sacramento California
Not listed San Diego California
Not listed San Francisco California
Not listed Boulder Colorado
Not listed Denver Colorado
Not listed Milford Connecticut
Not listed Boca Raton Florida
Not listed Bradenton Florida
Not listed Daytona Beach Florida
Not listed Delray Beach Florida
Not listed Fort Lauderdale Florida
Not listed Fort Myers Florida
Not listed Kissimmee Florida
Not listed Largo Florida
Not listed Miami Florida
Not listed Naples Florida
Not listed Orlando Florida
Not listed Palm Beach Gardens Florida
Not listed Sarasota Florida
Not listed St. Petersburg Florida
Not listed Sunrise Florida
Not listed Tampa Florida
Pain and Rehabilitation Clinic of Chicago Chicago Illinois 60610
Not listed Chicago Illinois
Not listed Towson Maryland
Not listed Boston Massachusetts
Not listed West Yarmouth Massachusetts
Not listed Southfield Michigan
Not listed Missoula Montana
Not listed Las Vegas Nevada
Not listed Brooklyn New York
Not listed High Point North Carolina
Not listed Winston-Salem North Carolina
Not listed Kettering Ohio
Not listed Bensalem Pennsylvania
Not listed Norristown Pennsylvania
Not listed Warwick Rhode Island
Not listed Dallas Texas

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00592774, 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 14, 2013 · Synced Jul 22, 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 NCT00592774 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →