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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00607256
Other study ID # A6061046
Secondary ID
Status Terminated
Phase Phase 3
First received
Last updated
Start date October 20, 2007
Est. completion date May 18, 2009

Study information

Verified date December 2019
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the lon-term safety and tolerability of [S,S]-reboxetine in patients with fibromyalgia


Recruitment information / eligibility

Status Terminated
Enrollment 500
Est. completion date May 18, 2009
Est. primary completion date May 18, 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Diagnosis of patients meeting the ACR criteria for fibromyalgia (i.e. widespread pain present for at least 3 months, and pain in at least 11 of 18 specific tender point sites)

Exclusion Criteria:

- Patients with other severe pain (e.g. DPN and PHN) that may confound assessment or self-evaluation of the pain associated with fibromyalgia

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
[S,S]-reboxetine
S_S reboxetine dosed daily.

Locations

Country Name City State
Belgium Pfizer Investigational Site Bruxelles
Belgium Pfizer Investigational Site Pellenberg
Canada Pfizer Investigational Site Kelowna British Columbia
Canada Pfizer Investigational Site Moncton New Brunswick
Canada Pfizer Investigational Site Pointe Claire Quebec
Canada Pfizer Investigational Site Sherbrooke Quebec
Czechia Pfizer Investigational Site Hlucin
Czechia Pfizer Investigational Site Pardubice
Czechia Pfizer Investigational Site Praha 2
Czechia Pfizer Investigational Site Zlin
France Pfizer Investigational Site Lille Cedex
France Pfizer Investigational Site Nice Cedex 1
France Pfizer Investigational Site Paris Cedex 04
Germany Pfizer Investigational Site Berlin
Germany Pfizer Investigational Site Berlin
Germany Pfizer Investigational Site Eichstaett
Germany Pfizer Investigational Site Goeppingen
Germany Pfizer Investigational Site Hamburg
Germany Pfizer Investigational Site Mannheim
Germany Pfizer Investigational Site Muenchen
Germany Pfizer Investigational Site Wiesbaden
Korea, Republic of Pfizer Investigational Site Gwangju
Korea, Republic of Pfizer Investigational Site Suwon-si Kyeongki-do
Netherlands Pfizer Investigational Site Breda
Netherlands Pfizer Investigational Site Emmen
Netherlands Pfizer Investigational Site Leeuwarden
South Africa Pfizer Investigational Site Boksburg Gauteng
South Africa Pfizer Investigational Site Panorama Western Cape
South Africa Pfizer Investigational Site Parow Western Cape
South Africa Pfizer Investigational Site Pretoria Gauteng Province
Sweden Pfizer Investigational Site Goteborg
Sweden Pfizer Investigational Site Molndal
Sweden Pfizer Investigational Site Stockholm
Sweden Pfizer Investigational Site Stockholm
United Kingdom Pfizer Investigational Site Cambridge
United Kingdom Pfizer Investigational Site Colchester
United Kingdom Pfizer Investigational Site Derby
United Kingdom Pfizer Investigational Site Dudley, West Midlands
United Kingdom Pfizer Investigational Site Greenock
United Kingdom Pfizer Investigational Site Paisley
United States Pfizer Investigational Site Anderson South Carolina
United States Pfizer Investigational Site Bethlehem Pennsylvania
United States Pfizer Investigational Site Cary North Carolina
United States Pfizer Investigational Site Charleston South Carolina
United States Pfizer Investigational Site Cincinnati Ohio
United States Pfizer Investigational Site Cranston Rhode Island
United States Pfizer Investigational Site Cumberland Rhode Island
United States Pfizer Investigational Site Denver Colorado
United States Pfizer Investigational Site Duncansville Pennsylvania
United States Pfizer Investigational Site Greer South Carolina
United States Pfizer Investigational Site Houston Texas
United States Pfizer Investigational Site Houston Texas
United States Pfizer Investigational Site Jacksonville Florida
United States Pfizer Investigational Site Jefferson City Missouri
United States Pfizer Investigational Site Kenilworth New Jersey
United States Pfizer Investigational Site Lake Jackson Texas
United States Pfizer Investigational Site Lexington Kentucky
United States Pfizer Investigational Site Lincoln Rhode Island
United States Pfizer Investigational Site Marion Ohio
United States Pfizer Investigational Site Medford Oregon
United States Pfizer Investigational Site Milwaukee Wisconsin
United States Pfizer Investigational Site Minot North Dakota
United States Pfizer Investigational Site Moline Illinois
United States Pfizer Investigational Site Ocala Florida
United States Pfizer Investigational Site Ocala Florida
United States Pfizer Investigational Site Orangevale California
United States Pfizer Investigational Site Prairie Village Kansas
United States Pfizer Investigational Site Richmond Virginia
United States Pfizer Investigational Site Rochester New York
United States Pfizer Investigational Site Saint Louis Missouri
United States Pfizer Investigational Site Salt Lake City Utah
United States Pfizer Investigational Site San Antonio Texas
United States Pfizer Investigational Site San Antonio Texas
United States Pfizer Investigational Site Santa Ana California
United States Pfizer Investigational Site Spokane Washington
United States Pfizer Investigational Site Staten Island New York
United States Pfizer Investigational Site Virginia Beach Virginia
United States Pfizer Investigational Site Warwick Rhode Island
United States Pfizer Investigational Site West Palm Beach Florida

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Countries where clinical trial is conducted

United States,  Belgium,  Canada,  Czechia,  France,  Germany,  Korea, Republic of,  Netherlands,  South Africa,  Sweden,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary 12-lead ECG 68 weeks
Primary Hematology/Biochemistry 68 weeks
Primary Adverse events 68 weeks
Primary Physical examination 68 weeks
Primary Vital signs 68 weeks
Secondary Patient Global Impression of Change 68 weeks
See also
  Status Clinical Trial Phase
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Recruiting NCT04554784 - Effectiveness of Bowen Therapy for Pain Management in Patients With Fibromyalgia N/A
Completed NCT03300635 - Metabolism, Muscle Function and Psychological Factors in Fibromyalgia N/A
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Completed NCT03227952 - Sensory Stimulation in Fibromyalgia N/A
Completed NCT03166995 - Postural Exercises in Women With Fibromyalgia N/A
Recruiting NCT06237595 - Vagus Nerve Stimulation in Fibromyalgia N/A
Completed NCT01888640 - Fibromyalgia Activity Study With Transcutaneous Electrical Nerve Stimulation (FAST) N/A
Completed NCT03641495 - Pain Education and Therapeutic Exercise for Fibromyalgia N/A
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Active, not recruiting NCT05128162 - Open-label Study to Assess the Safety and Efficacy of Psilocybin With Psychotherapy in Adult Participants With Fibromyalgia Phase 2
Completed NCT04674878 - Comparison of Muscle Energy Techniques and Breathing Exercises for Functional Improvement in Fibromyalgia N/A
Active, not recruiting NCT04084795 - Augmentation of EMDR With tDCS in the Treatment of Fibromyalgia N/A
Completed NCT03129906 - Impact of the Restriction of Sources of Gluten in Fibromyalgia Patients N/A
Completed NCT05058911 - Exposure-based Cognitive Behavior Therapy vs Traditional Cognitive Behavior Therapy for Fibromyalgia N/A
Recruiting NCT04571853 - New Educational Tool for FM N/A
Recruiting NCT04571528 - Effectiveness of VIRTUAL FIBROWALK STUDY N/A