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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 Oct 22, 2026, 11:13 PM 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

Brief summary

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

Study objective is to assess the safety and effectiveness of once- daily GRALISE 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
Sep 2011 (Type not available)
Primary completion
Mar 2012 (Actual)
Completion
Apr 2012 (Actual)
Last update posted
Mar 21, 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 21, 2013 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01426230 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →