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Terminated Phase 2 Interventional Results available

A Study Evaluating Desvenlafaxine Sustained Release (DVS SR) in Adult Female Outpatients With Fibromyalgia

ClinicalTrials.gov ID: NCT00696787

Public ClinicalTrials.gov record NCT00696787. 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 May 12, 2026, 10:02 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled, Pregabalin-Referenced, Parallel-Group, Adaptive Design Study of DVS SR in Adult Female Outpatients With Fibromyalgia Syndrome

Study identification

NCT ID
NCT00696787
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Enrollment
125 participants

Conditions and interventions

Conditions

Interventions

  • Desvenlafaxine Sustained Release (DVS SR) Drug
  • Lyrica® (Pregabalin) Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
May 31, 2008
Primary completion
Dec 31, 2008
Completion
Dec 31, 2008
Last update posted
Feb 24, 2013

2008 – 2009

United States locations

U.S. sites
27
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
Not listed Huntsville Alabama 35801
Not listed Roseville California 95661
Not listed San Diego California 92108
Not listed San Diego California 92128
Not listed Santa Ana California 92705
Not listed Walnut Creek California 94598
Not listed Jacksonville Florida 32216
Not listed Tampa Florida 33606
Not listed Decatur Georgia 30033
Not listed Evansville Indiana 47714
Not listed Indianapolis Indiana 46260
Not listed Lexington Kentucky 40509
Not listed Rockville Maryland 20852
Not listed Lansing Michigan 48910
Not listed Raleigh North Carolina 27612
Not listed Cincinnati Ohio 45219
Not listed Dayton Ohio 45408
Not listed Duncansville Pennsylvania 16635
Not listed Philadelphia Pennsylvania 19152
Not listed Chattanooga Tennessee 37404
Not listed Chattanooga Tennessee 37421
Not listed Knoxville Tennessee 37920
Not listed Austin Texas 78756
Not listed Dallas Texas 75231
Not listed San Antonio Texas 78205
Not listed Salt Lake City Utah 84102
Not listed Middleton Wisconsin 53562

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 NCT00696787, 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 Feb 24, 2013 · Synced May 12, 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 NCT00696787 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →