Fibromyalgia, Primary Clinical Trial
— FrIDAyOfficial title:
Observation of Patients Affected by Fibromyalgic Syndrome (FMS): Comparison of Different Therapeutic Approaches
Verified date | September 2019 |
Source | Azienda Ospedaliera Universitaria Integrata Verona |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Fibromyalgia or Fibromyalgic Sindrome (FMS) is a chronic debilitating pain syndrome,
characterized by widespread chronic musculoskeletal pain and generalized painful
hypersensitivity, which may be associated with systemic, cognitive and psycho-emotional
somatic disorders. Etiology is not completely known. The diagnosis of fibromyalgia is
anamnestic and clinical, without evident alterations at the objective examination or at
laboratory and radiology investigations. According last guidelines, the best approach to
treat FMS must be personalized and multidisciplinary, including pharmacological and
non-pharmacological interventions. Moreover, a correct treatment of comorbidities, practice
of bland physical activity or meditative discipline, as well as a pychological support are
very important in FMS.
The aim of this study is to evaluate the activity of some common therapeutic pathways
available for FMS: acupuncture and nutraceutical products; the latter are numerous on the
market and based on powerful antioxidants. In this case Migratens was chosen for its
composition: α-lipoic acid, polyvitaminic complexes (B and D group vitamins), coenzyme Q10,
magnesium and tryptophan.
Status | Enrolling by invitation |
Enrollment | 61 |
Est. completion date | December 30, 2020 |
Est. primary completion date | December 30, 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 30 Years to 65 Years |
Eligibility |
Inclusion Criteria: - patients not under pharmacological treatment for at least six months, - patients with a new diagnosis of fibromyalgia (FM) - hypovitaminosis D (vitamin D <30 mg / ml) or patients already in oral supplementation with 1,000 IU / day. People with hypovitaminosis are treated with Vitamin D supplementation - 30 - 65 years old - female sex - signature of informed consent Exclusion Criteria: - patients treated with active drugs on the neuroendocrine system - intake of drugs that can influence skeletal metabolism - addition of other fibromyalgia medicines other than those included in the study, during the observational period - allergies to components of the food supplement used - use of oral hypoglycemic agents - participation in other studies - recent acupuncture treatments elsewhere - severe psychiatric or neurological disorders |
Country | Name | City | State |
---|---|---|---|
Italy | Nrc | Verona | Italia |
Lead Sponsor | Collaborator |
---|---|
Vittorio Schweiger |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | visual analogue scale pain reduction in fibromyalgic patients from baseline to 6 months follow-up | to observe pain reduction in fibromyalgic patients treated with nutraceutic (Migratens®) - Groupo A, and with acupuncture - Group B, at the end of the study. visual analogue scale is anagogic scale that evaluate continuous aspect of the scale differentiates it from discrete scales such as the Likert scale, from 0 to 10. | 6 months | |
Secondary | visual analogue scale pain reduction in fibromyalgic patients from baseline to 1 month follow-up, from baseline to 3 months follow-up | - to observe pain reduction in fibromyalgic patients treated with nutraceutic (Migratens®) - Groupo A, and with acupuncture - Group B, at different follow up time visual analogue scale is anagogic scale that evaluate continuous aspect of the scale differentiates it from discrete scales such as the Likert scale, from 0 to 10. | 1 and 3 months | |
Secondary | Cenestesi improvement measured with revised Fibromyalgia Impact Questionnaire SCORE in fibromyalgic patients from baseline to 6 months follow-up | to value general improvement of cenestesi between two groups. each of the 9 questiona of questionnaire present a score from 0 to 10 to evaluate haw fibromyalgia make activities difficult, zero score correspond to no difficult and 10 to always difficult. | 6 months | |
Secondary | visual analogue scale pain reduction in fibromyalgic patients from 3 month to 6 month | to observe time of pain reduction or pain free after treatment end. visual analogue scale is anagogic scale that evaluate continuous aspect of the scale differentiates it from discrete scales such as the Likert scale, from 0 to 10. | 3 and 6 months | |
Secondary | percentage of adverse effect | to observe number and type of treatment adverse effect during study time | 6 months |
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