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Completed No phase listed Observational Results available

Phase IV Study of FDA Approved, Once-Daily GRALISE™(Gabapentin) Tablets for the Treatment of Postherpetic Neuralgia

ClinicalTrials.gov ID: NCT01426230

Public ClinicalTrials.gov record NCT01426230. 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 21, 2026, 7:02 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 Phase 4, Open Label, Study of Safety and Effectiveness of GRALISE™(Gabapentin) Tablets in the Treatment of Patients With Postherpetic Neuralgia in Clinical Practice

Study identification

NCT ID
NCT01426230
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Depomed
Industry
Enrollment
201 participants

Conditions and interventions

Interventions

Not listed

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
Aug 31, 2011
Primary completion
Feb 29, 2012
Completion
Mar 31, 2012
Last update posted
Mar 20, 2013

2011 – 2012

United States locations

U.S. sites
37
U.S. states
19
U.S. cities
37
Facility City State ZIP Site status
Not listed Mobile Alabama
Not listed Tuscaloosa Alabama
Not listed Phoenix Arizona
Not listed Sun City Arizona
Not listed Tucson Arizona
Not listed Fresno California
Not listed San Francisco California
Not listed Fairfield Connecticut
Not listed Lauderdale Lakes Florida
Not listed Naples Florida
Not listed North Palm Beach Florida
Not listed Ormond Beach Florida
Not listed Palm Beach Florida
Not listed Sunrise Florida
Not listed Marietta Georgia
Not listed Bolingbrook Illinois
Not listed Evansville Indiana
Not listed Lexington Kentucky
Not listed Brighton Massachusetts
Not listed Worcestor Massachusetts
Not listed Jefferson City Missouri
Not listed St Louis Missouri
Not listed Tom River New Jersey
Not listed Hickory North Carolina
Not listed Raleigh North Carolina
Not listed Allentown Pennsylvania
Not listed Altoona Pennsylvania
Not listed Wyomissing Pennsylvania
Not listed Mt. Pleasant South Carolina
Not listed Cordova Tennessee
Not listed Austin Texas
Not listed Bedford Texas
Not listed Corpus Christi Texas
Not listed Houston Texas
Not listed San Antonio Texas
Not listed Orem Utah
Not listed Edmonds Washington

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 NCT01426230, 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 Mar 20, 2013 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01426230 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →