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Completed Phase 3 Interventional Results available

Study of Gabapentin Extended Release (G-ER) in the Treatment of Vasomotor (Hot Flashes/Hot Flushes) Symptoms in Postmenopausal Women

ClinicalTrials.gov ID: NCT00755417

Public ClinicalTrials.gov record NCT00755417. 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 27, 2026, 5:11 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 3 Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Safety and Efficacy of Gabapentin Extended Release (G-ER) Tablets in the Treatment of Vasomotor Symptoms in Postmenopausal Women

Brief summary

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

Depomed's Gabapentin Extended Release (G-ER) is an investigational, extended release formulation of gabapentin that is being studied for the treatment of hot flashes in postmenopausal women.

Study identification

NCT ID
NCT00755417
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Depomed
Industry
Enrollment
541 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
Female
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 2008 (Type not available)
Primary completion
Aug 2009 (Actual)
Completion
Oct 2009 (Actual)
Last update posted
Mar 7, 2012

2008 – 2009

United States locations

U.S. sites
45
U.S. states
25
U.S. cities
45
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Montgomery Alabama — —
Not listed Tempe Arizona — —
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Not listed Clearwater Florida — —
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Not listed New Port Richey Florida — —
Not listed Orlando Florida — —
Not listed St. Petersburg Florida — —
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Not listed Atlanta Georgia — —
Not listed Sandy Springs Georgia — —
Not listed Savannah Georgia — —
Not listed Chicago Illinois — —
Not listed Madisonville Kentucky — —
Not listed Fall River Massachusetts — —
Not listed Edina Minnesota — —
Not listed St Louis Missouri — —
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Not listed Moorestown New Jersey — —
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Not listed Fargo North Dakota — —
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Not listed West Reading Pennsylvania — —
Not listed Columbia South Carolina — —
Not listed Hilton Head Island South Carolina — —
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Not listed Dallas Texas — —
Not listed Houston Texas — —
Not listed San Antonio Texas — —
Not listed Salt Lake City Utah — —
Not listed Bellevue Washington — —
Not listed Renton Washington — —
Not listed Spokane 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 NCT00755417, 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 7, 2012 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00755417 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →