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Fibromyalgia, PrimaryFrIDAyNCT04098757

Fibromyalgia Different Approaches: Acupuncture vs Migratens

An observational study of Fibromyalgia, Primary and Fibromyalgic Sindrome, run by Vittorio Schweiger at 1 site in Italy.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 30 to 65 years, women only
Conditions the study is for
Fibromyalgia, Primary, Fibromyalgic Sindrome
What is being tested?
Migratens
How many people
61 participants
Where
1 siteItaly
Study dates
1 Jan 2019to 30 Dec 2020
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 30 to 65 years
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients suffering from fibromyalgia for at least 6 months according to the modified criteria of 2016 affering to Verona's Hospital

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • Nrc

    Verona, Italia, 37134

Other trials in Italy

About this study

Official title: Observation of Patients Affected by Fibromyalgic Syndrome (FMS): Comparison of Different Therapeutic Approaches

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.

Read the detailed description

Fibromyalgia or Fibromyalgic Sindrome (FMS) is a chronic debilitating pain syndrome, affecting about 2-4% of the general population, with an average peak between 30 and 50 years, but with a significantly higher prevalence, until about 8-10%, if considered only female sex or greater age. Fibromyalgia is characterized by the presence of widespread chronic musculoskeletal pain and generalized painful hypersensitivity, which may be associated with systemic, cognitive and psycho-emotional somatic disorders, such as: asthenia, sleep disorders, depression, anxiety, headache, paresthesia, dry eye, tachycardia, intercostal pain, dyspnoea, gastrointestinal or gynecological or urological disorders.

Etiology is not completely known, even if genetic, environmental, physical and emotional factors seem to interact and promote an hypersensitive state, both at central and peripheral level, leading to a functional disorder of pain modulation system. Sleep or immune system disorders, focal tissue abnormalities, physical or psychological trauma seem to trigger the disease, but many patients are not able to identify any apparent cause.

Validated questionnaires, including the Fibromyalgia Impact Questionnaire (FIQ), are used to assess the impact of fibromyalgia on people's health and quality of life; in 2016 this survey was revised (FIQR) to intercept almost the entire spectrum (domains) of problems related to the disease and response to treatment, as well as to include other relevant parameters in the evaluation of the FMS patient (eg assessment of cognitive functions, balance problems, etc.), absent in the original version. In this scale the score of each item ranges from 0 to 10. First block of questions concerns the physical function of the subject and the related physical difficulties experienced in the last week; the subtotal score of first 9 items is divided by three, therefore the maximum score is 30. Second domain concerns FMS impact on general health in the last week and consists of two questions; the relative score remains unchanged, so maximum score is 20. Third domain consists of 10 items concerning the severity of main symptoms related to fibromyalgia experienced in the last week; addition of these is divided by two, thus maximum score is 50. Sum of all three domains corresponds to the total of the questionnaire and its interpretation is as follows: 0-42 mild FMS, 43-59 moderate FMS, 60-74 severe FMS, 75-100 FMS very serious. In this survey also depression is valuated, in a scale from 0 (absence of mood disorder) to 10 (severe depression).

Visual Analogue Scale (VAS) is a visual representation of severity of pain felt by the patient, indicated on a 10 cm long line, where one end indicates the absence of ache (0), while the other corresponds to the worst pain imaginable (10).

According last guidelines, the best approach to treat FMS must be personalized and multidisciplinary, including pharmacological and non-pharmacological interventions. Drugs, with off-label indication for fibromyalgia, are amitriptyline, duloxetine and pregabalin, in monotherapy or combined. If there is no response, patients may try to employ analgesics and anti-inflammatories as needed or use complementary and alternative therapies (for example: acupuncture, transcranial stimulation or TENS, cannabinoid derivatives, nutraceutical products, vitamin D supplementation). 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 first one involves treating the most painful areas with local, adjacent and distant points, as well as treating basic condition, framed according to Traditional Chinese Medicine (TCM). In clinical practice, selection of acupoints must be based on diagnostic criteria of TCM and aimed to reduce symptoms, therefore it must be personalized as much as possible, even if some points of treatment are more frequent. Metal needles, placed into specific acupoints, modulate the release of various pain neuromediators (serotonin, substance P, neuro peptide Y, endorphins), in addition to activate a local and systemic anti-inflammatory effect, with further sedative properties on pain. Moreover, there are evidences that acupuncture enhances the effect of pharmacological treatment (antidepressants) and exercise on pain reduction of 30% (30 points on a pain scale from 0 to 100), with almost null adverse effects.

Numerous nutraceutical products for fibromyalgia are available on the market; among these Migratens was chosen for its composition: in fact it contains α-lipoic acid, a powerful endogenous antioxidants, polyvitaminic complexes (B and D group vitamins) and coenzyme Q10, essential for correct cellular functionality, magnesium and tryptophan, mineral and essential aminoacid with positive effects on skeletal muscle system, sleep and mood disorders.

This study expects to evaluate which of these treatment, acupuncture and nutraceutical products, allow a pain reduction, but also an improvement of general well-being, with positive effects on somatic or psycho-emotional symptoms, without significant side effects added.

WPI, SSS, Fibromyalgia Impact Questionnaire-Revised (FIQR), Visual Analogic Scale are instrument to estimate FMS severity at different time: at the fist patient evaluation, during treatment time and at the end of the study, after at least three month free from therapy.

Sixty-one female fibromyalgic patients were recruited for this study and randomized for the two possible treatments: 27 of them were assigned to Group A, for a therapy of three months with Migratens (2 sachets/day), and 34 to Group B, treated with ten (one cycle) or twenty (two cycles, with a month break between cycles) acupuncture sessions, carried out by the same operator. The subjects assigned to the two groups follow the normal controls, during which the participants have to indicate number, type and dosage of the symptomatic drugs taken in a daily allowance. Another check will also be performed at six months from the beginning of enrollment, after at least three months free of treatment. In fact, it is interesting to understand which therapeutic strategy is most effective and which one presents a more lasting pain reduction over time from the end of treatment to the subsequent follow-up.

Being tested
Migratens
Keywords
Fibromyalgia, Fibromyalgic Sindrome (FMS), Pain, Acupuncture, Nutraceutical products
Medical subject headings
Fibromyalgia, Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MigratensDietary supplement

    2 sachets/day: 800 mg of α-Lipoic acid, 450 mg of magnesium bisglycinate, 300 mg of L-Tryptophan, 20 mcg of Vitamin D3, 2.4 mg of Vitamin B2, 25 mg of Niacin, 150 mg of Coenzyme Q10. Patients who receive Migratens food supplementation have to take 2 sachets / day for 12 weeks. The supplement will be prescribed as usual and the assumption of the same will be recorded by partecipants in the appropriate daily; if the subject does not continue the indication the data collected up to that moment will be considered.

Study groups in NCT04098757
Study groupRoleWhat they receive
Migratens2 sachets/day: 800 mg of α-Lipoic acid, 450 mg of magnesium bisglycinate, 300 mg of L-Tryptophan, 20 mcg of Vitamin D3, 2.4 mg of Vitamin B2, 25 mg of Niacin, 150 mg of Coenzyme Q10. Patients who receive Migratens food supplementation have to take 2 sachets / day for 12 weeks. The supplement will be prescribed as usual and the assumption of the same will be recorded by partecipants in the appropriate daily; if the subject does not continue the indication the data collected up to that moment will be considered.
Receives: Dietary Supplement: Migratens
acupuncture2 sessions a week, for a total of 10 (5 weeks), performed by the same operator, repeatable if necessary, after a therapeutic interval of at least one month. Each session lasts about 20-30 minutes per patient. Tewa J Type sterile disposable needles, coated, with a Chinese-style copper wire handle, with a guide tube, of 22x13 mm (CJ 2213) and 30x25 mm (CJ 3025) will be used. Acupuncture will be carried out by same trained operator.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.

    Measured: 6 months

Secondary outcomes (4)
  1. 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.

    Measured: 1 and 3 months

  2. 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.

    Measured: 6 months

  3. 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.

    Measured: 3 and 6 months

  4. percentage of adverse effect

    to observe number and type of treatment adverse effect during study time

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Sep 2019
  2. Study start1 Jan 2019
  3. Primary completion30 Dec 2020 (estimated)
  4. Study completion30 Dec 2020 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
61 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04098757
Sponsor's protocol ID
1917CESC FrIDAy
Acronym
FrIDAy
Status last verified
Sep 2019
First submitted
18 Feb 2019
Last updated
23 Sep 2019
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Fibromyalgia, Primary and Fibromyalgic Sindrome, run by Vittorio Schweiger at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 23 Sep 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

visual analogue scale pain reduction in fibromyalgic patients from baseline to 6 months follow-up (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Sep 2019.

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