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.
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.
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.
- Conditions
- Fibromyalgia, Primary, Fibromyalgic Sindrome
- 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 group | Role | What they receive |
|---|---|---|
| Migratens | 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. Receives: Dietary Supplement: Migratens | |
| acupuncture | 2 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.
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)
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
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
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
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.
- First posted23 Sep 2019
- Study start1 Jan 2019
- Primary completion30 Dec 2020 (estimated)
- Study completion30 Dec 2020 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Fibromyalgia, PrimaryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Vittorio Schweiger
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Vittorio Schweiger, Azienda Ospedaliera Universitaria Integrata Verona
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
Study at a glance
From the registry record, last updated by the sponsor on 23 Sep 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Observation of Patients Affected by Fibromyalgic Syndrome (FMS): Comparison of Different Therapeutic Approaches
- ClinicalTrials.gov ID
- NCT04098757
- Acronym / sponsor ID
- FrIDAy / 1917CESC FrIDAy
- Conditions
- Fibromyalgia, Primary, Fibromyalgic Sindrome
- Keywords
- Fibromyalgia, Fibromyalgic Sindrome (FMS), Pain, Acupuncture, Nutraceutical products
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 61 participants (actual)
- Lead sponsor
- Vittorio SchweigerUniversity, hospital or other
- Study start
- 1 Jan 2019 (actual)
- Primary completion
- 30 Dec 2020 (estimated)
- Study completion
- 30 Dec 2020 (estimated)
- First posted
- 23 Sep 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Migratens | – | Dietary Supplement: 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. |
| acupuncture | – | –2 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. |
Who may qualify
- Ages
- 30 to 65 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- 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
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (8 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| 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. | Dietary supplement | Migratens |
Primary outcome
visual analogue scale pain reduction in fibromyalgic patients from baseline to 6 months follow-up
Time frame: 6 months
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.
4 secondary outcomes
visual analogue scale pain reduction in fibromyalgic patients from baseline to 1 month follow-up, from baseline to 3 months follow-up
Time frame: 1 and 3 months
Cenestesi improvement measured with revised Fibromyalgia Impact Questionnaire SCORE in fibromyalgic patients from baseline to 6 months follow-up
Time frame: 6 months
visual analogue scale pain reduction in fibromyalgic patients from 3 month to 6 month
Time frame: 3 and 6 months
percentage of adverse effect
Time frame: 6 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Sep 2019.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.