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Terminated Phase 2 Interventional

A Trial Assessing The Long Term Safety And Tolerability Of [S,S]-Reboxetine In Patients With Post-Shingles Pain.

ClinicalTrials.gov ID: NCT00353808

Public ClinicalTrials.gov record NCT00353808. 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 Oct 24, 2026, 4:13 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

An Open-Label Extension Trial Assessing The Safety And Tolerability Of [S,S]-Reboxetine In Patients With Postherpetic Neuralgia (PHN).

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the long-term safety and tolerability of \[S,S\]-Reboxetine in patients with chronic pain following shingles. This is the extension study of Protocol A6061026.

Study identification

NCT ID
NCT00353808
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
112 participants

Conditions and interventions

Conditions

Interventions

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
Jul 2006 (Type not available)
Primary completion
Not listed
Completion
Oct 2007 (Actual)
Last update posted
Apr 7, 2011

2006 – 2007

United States locations

U.S. sites
57
U.S. states
22
U.S. cities
56
Facility City State ZIP Site status
Pfizer Investigational Site Huntsville Alabama 35801 —
Pfizer Investigational Site Chandler Arizona 85225 —
Pfizer Investigational Site Gilbert Arizona 85234 —
Pfizer Investigational Site Sun City Arizona 85351 —
Pfizer Investigational Site Tucson Arizona 85741 —
Pfizer Investigational Site Arcadia California 91007 —
Pfizer Investigational Site Fullerton California 92835 —
Pfizer Investigational Site Irvine California 92618 —
Pfizer Investigational Site Laguna Hills California 92653 —
Pfizer Investigational Site Loma Linda California 92354 —
Pfizer Investigational Site Redondo Beach California 90277 —
Pfizer Investigational Site Boulder Colorado 80304 —
Pfizer Investigational Site Clearwater Florida 33765 —
Pfizer Investigational Site Fort Myers Florida 33912 —
Pfizer Investigational Site Holly Hill Florida 32117 —
Pfizer Investigational Site Hollywood Florida 33021 —
Pfizer Investigational Site Kissimmee Florida 34741 —
Pfizer Investigational Site Largo Florida 33770 —
Pfizer Investigational Site Longwood Florida 32779 —
Pfizer Investigational Site Ocala Florida 34471 —
Pfizer Investigational Site Ormond Beach Florida 32174 —
Pfizer Investigational Site Palm Beach Gardens Florida 33418 —
Pfizer Investigational Site Chicago Illinois 60610 —
Pfizer Investigational Site Oak Brook Illinois 60523 —
Pfizer Investigational Site Topeka Kansas 66606 —
Pfizer Investigational Site Ruston Louisiana 71270 —
Pfizer Investigational Site Towson Maryland 21286 —
Pfizer Investigational Site Boston Massachusetts 02215 —
Pfizer Investigational Site Brockton Massachusetts 02301 —
Pfizer Investigational Site Ann Arbor Michigan 48104 —
Pfizer Investigational Site Independence Missouri 64055 —
Pfizer Investigational Site Kansas City Missouri 64114 —
Pfizer Investigational Site Nixa Missouri 65714 —
Pfizer Investigational Site Springfield Missouri 65807 —
Pfizer Investigational Site St Louis Missouri 63141 —
Pfizer Investigational Site Amherst New York 14226 —
Pfizer Investigational Site New York New York 10003 —
Pfizer Investigational Site Orchard Park New York 14127 —
Pfizer Investigational Site Asheville North Carolina 28806 —
Pfizer Investigational Site Raleigh North Carolina 27607-6520 —
Pfizer Investigational Site Winston-Salem North Carolina 27103 —
Pfizer Investigational Site Fargo North Dakota 58103 —
Pfizer Investigational Site Canfield Ohio 44406 —
Pfizer Investigational Site Kettering Ohio 45429 —
Pfizer Investigational Site Youngstown Ohio 44504 —
Pfizer Investigational Site Oklahoma City Oklahoma 73112 —
Pfizer Investigational Site Allentown Pennsylvania 18103 —
Pfizer Investigational Site Altoona Pennsylvania 16602 —
Pfizer Investigational Site Duncansville Pennsylvania 16635-0909 —
Pfizer Investigational Site Jackson Tennessee 38305 —
Pfizer Investigational Site Dallas Texas 75230 —
Pfizer Investigational Site Houston Texas 77024 —
Pfizer Investigational Site Houston Texas 77063 —
Pfizer Investigational Site San Antonio Texas 78229 —
Pfizer Investigational Site Richmond Virginia 23294 —
Pfizer Investigational Site Spokane Washington 99204 —
Pfizer Investigational Site Tacoma Washington 98405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00353808, 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 Apr 7, 2011 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00353808 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →