Fibromyalgia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women, less than 65 years old, non-pregnant, non-brest feeding Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: Symptoms or signs of rheumatoid arthritis, multiple sclerosis, malignancy, or other serious disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: To test the hypothesis that injections of sterile water in the tenderpoints relieves the pain symptoms during at least one year;Secondary Objective: The pain relief is caused by a "resetting" of the nosoceptors, in turn caused by changes in the release of neuropeptides;Primary end point(s): Number of tenderpoints, arm abduction test, chair raising test, and a set of quality of life measures | — |
Countries
Sweden