Study of Fibromyalgia Treated With Milnacipran

PHASE4CompletedINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

May 31, 2010

Primary Completion Date

January 31, 2013

Study Completion Date

January 31, 2013

Conditions
Fibromyalgia
Interventions
DRUG

Milnacipran

Subject with Fibromyalgia will then be titrated onto milnacipran over 8 days to subject reported optimal pain control or a maximal dose of 100mg/day per package insert. Subjects will be permitted to increase or decrease their dosing at any time during the study per MD discretion in order to maintain optimal pain control.

PROCEDURE

Skin biopsy

Subjects with Fibromyalgia will have 3 mm skin biopsies obtained from the dominant trapezius and the glabrous hypothenar area of the hand.

PROCEDURE

Skin Biopsy

Control Subjects will have 3 mm skin biopsies obtained from the dominant trapezius and the glabrous hypothenar area of the hand.

Trial Locations (1)

12205

Upstate Clinical Research, LLC, Albany

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Forest Laboratories

INDUSTRY

lead

Albany Medical College

OTHER