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Completed Phase 4 Interventional Results available

Randomized Study Comparing the Efficacy and Safety of Varenicline Tartrate to Placebo in Smoking Cessation When Subjects Are Allowed to Set Their Own Quit Date

ClinicalTrials.gov ID: NCT00691483

Public ClinicalTrials.gov record NCT00691483. 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 24, 2026, 12:38 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, Prospective, Multi-National, Randomized, Double-Blind, Placebo-Controlled Study To Evaluate Smoking Cessation With Varenicline Tartrate Compared With Placebo In The Setting Of Patient Self-Selected (Flexible) Quit Date

Study identification

NCT ID
NCT00691483
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Pfizer
Industry
Enrollment
659 participants

Conditions and interventions

Interventions

  • placebo Drug
  • varenicline Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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, 2008
Primary completion
Aug 31, 2009
Completion
Nov 30, 2009
Last update posted
Nov 19, 2015

2008 – 2009

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Pfizer Investigational Site Litchfield Park Arizona 85340
Pfizer Investigational Site Los Angeles California 90095
Pfizer Investigational Site Santa Ana California 92705
Pfizer Investigational Site Overland Park Kansas 66212
Pfizer Investigational Site Lexington Kentucky 40509
Pfizer Investigational Site Milford Massachusetts 01757
Pfizer Investigational Site Omaha Nebraska 68116-2004
Pfizer Investigational Site Endwell New York 13760
Pfizer Investigational Site Bridgeville Pennsylvania 15017
Pfizer Investigational Site Philadelphia Pennsylvania 19146
Pfizer Investigational Site Nashville Tennessee 37203
Pfizer Investigational Site Houston Texas 77030

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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00691483, 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 Nov 19, 2015 · Synced Jul 24, 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 NCT00691483 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →