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Fibromyalgia (FM)SHD-FMNCT07293767

Silymarin vs Hesperidin/Diosmin in Fibromyalgia

A study testing Silymarin (LEGALON) and Diosmin / Hesperidin (Daflon) in people with Fibromyalgia (FM), run by Ain Shams University at 1 site in Egypt.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Fibromyalgia is a chronic disease, characterized by chronic widespread pain, physical exhaustion, sleep problems, and unexplained pain in both joints and muscles. Fibromyalgia's causes still unknown, but there are various risk factors that can cause fibromyalgia such as genetic causes, physical shock, and infections. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Fibromyalgia (FM)
What is being tested?
Silymarin (LEGALON) and Diosmin / Hesperidin (Daflon)
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
90 participants
Where
1 siteEgypt
Study dates
16 Nov 2024to 31 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 18 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Informed written consent.
  • Participant must meet the American College of Rheumatology 2016 revised classification criteria for Fibromyalgia: Widespread pain index (WPI) ≥ 7 and symptom severity (SS) scale score ≥ 5, or WPI 3 to 6 and SS scale score ≥ 9
  • Age >18 years old (males and females)
  • Diagnosis of FM confirmed by a rheumatologist.
  • Persistent pain syndrome on conventional therapy.
  • Not taking Daflon or Legalon for 6 months.

Who cannot join

  • Pain due to other conditions (e.g. diabetic peripheral neuropathic pain or post-herpetic neuralgia) that would confound assessment or self-evaluation of the pain associated with FM.
  • Patients with pain due to any widespread inflammatory musculoskeletal disorder (e.g. rheumatoid arthritis, lupus) or widespread rheumatic disease other than FM.
  • Allergy to silymarin or diosmin or hesperidin.
  • Cognitive deficits that could impair understanding of the study, completion of questionnaires, or adherence to therapy.
  • Pregnant or planning pregnancy women and breastfeeding women.
  • Major comorbidities like renal impairment, severe liver disease, chronic hepatitis C, history of alcohol or drug addiction.
  • Current severe or uncontrolled major depressive disorder or anxiety disorders.
  • Patients will be excluded if there is no compliance to the medication.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

menna s teaching assistant of clinical pharmacy/ master's student contact

01064897439

mssalama@msa.edu.eg

Egypt1 site, 1 recruiting
  • Outpatients clinic of department of Internal medicine- Rheumatology unit Ain shams hospitals.

    Cairo

    mennaallah sayed s teaching assistant of clinical pharmacy/ master's student, master's, 01064897439 ext. 01000132431, mssalama@msa.edu.eg

    nagwa ali A Professor of clinical pharmacy, 01223411984, nagwa.sabri@pharma.asu.edu.eg

    Recruiting

Other trials in Egypt

About this study

Official title: The Effect of Silymarin Versus Hesperidin/Diosmin Combination on Patients With Fibromyalgia

Fibromyalgia is a chronic disease, characterized by chronic widespread pain, physical exhaustion, sleep problems, and unexplained pain in both joints and muscles. Fibromyalgia's causes still unknown, but there are various risk factors that can cause fibromyalgia such as genetic causes, physical shock, and infections. Fibromyalgia typically presents in young or middle aged females, it occurs in females more than males, and it is characterized with widespread pain throughout the whole body in both sides such as arms, shoulders, head, and abdominal areas. The etiology of fibromyalgia still unclear, but there are several factors such as alterations in the sleep pattern, changes in the neuroendocrine transmitters such as cortisol, growth hormones and serotonin, dysfunction of central and autonomic nervous systems, psychiatric aspects and external stressors . The pain seems to result from neurochemical imbalances in the central nervous system that lead to a "central amplification" of pain perception characterized by allodynia (a heightened sensitivity to stimuli that are not normally painful) and hyperalgesia (an increased response to painful stimuli). this interventional study aims to study effect of silymarin and hesperidin/diosmin combination on fibromyalgia patients and compare their effect with control patients on the following

  1. Management of pain.
  2. Inflammatory biomarkers.
  3. Quality of life.
Read the detailed description

Fibromyalgia is a chronic disease characterized by chronic widespread pain, physical exhaustion, sleep problems, and unexplained pain in joints and muscles. Although the exact causes remain unknown, several risk factors have been implicated, including genetic predisposition, physical or emotional stress, and infections. Fibromyalgia occurs predominantly in females and is associated with widespread pain in multiple body regions such as the arms, shoulders, head, and abdomen. The etiology involves alterations in sleep patterns, changes in neuroendocrine transmitters such as cortisol, growth hormone, and serotonin, along with dysfunction of the central and autonomic nervous systems. Pain is believed to result from neurochemical imbalances that lead to central amplification of pain perception, characterized by allodynia and hyperalgesia.

Diagnosis of fibromyalgia is challenging, as no specific laboratory tests or imaging confirm the condition. The 1990 ACR criteria relied on tender points and widespread pain for at least three months. More recently, the ACR proposed new diagnostic criteria incorporating the Widespread Pain Index (WPI) and Symptom Severity (SS) scale, which evaluate pain in 19 body regions and rate associated symptoms such as fatigue, cognitive difficulties, headache, and dizziness.

Management of fibromyalgia includes several approaches. FDA-approved medications include pregabalin, duloxetine, and milnacipran, although these may be costly and associated with side effects. Anticonvulsants, amitriptyline, and fluoxetine may also be used to improve pain and sleep. Non-pharmacological therapies include biofeedback, cognitive behavioral therapy, physiotherapy, exercise, and electromyogram-guided interventions. Alternative therapies such as acupuncture, chiropractic care, deep tissue massage, neuromuscular massage, meditation, and certain herbal supplements (e.g., echinacea purpurea, black cohosh, lavender, Silybum marianum) have shown varying degrees of benefit.

Inflammatory mediators, particularly IL-6 and IL-8, are commonly elevated in fibromyalgia and correlate with functional impairment, fatigue, and sleep disturbance. Silymarin, extracted from Silybum marianum, possesses hepatoprotective, antioxidant, anti-inflammatory, immunomodulatory, and cardioprotective activities. It has demonstrated reductions in inflammatory cytokines such as TNF-α and IL-6 and showed significant reduction of IL-1α and IL-8 in clinical studies. Diosmin/hesperidin, a flavonoid combination derived from citrus fruits, also exhibits antioxidant and anti-inflammatory activity and has produced antihyperalgesic effects in neuropathic pain models through the reduction of TNF-α, IL-1β, and IL-6.

Based on these findings, the current study hypothesizes that administering silymarin or diosmin/hesperidin in addition to standard fibromyalgia therapy may reduce inflammation and improve pain outcomes in patients with fibromyalgia. The study will compare the effects of silymarin versus diosmin/hesperidin on clinical symptoms, inflammatory biomarkers, and quality of life over a four-month period, as well as evaluate their safety and tolerability.

Being tested
Silymarin (LEGALON), Diosmin / Hesperidin (Daflon), no intervention (control group)
Keywords
fibromyalgia, silymarin, hesperidin, diosmin
Medical subject headings
Fibromyalgia

What participants receive

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

  • Silymarin (LEGALON)Drug

    oral silymarin (legalon) 140 mg will be taken 3 times daily for 12 weeks with the standard treatment

  • Diosmin / Hesperidin (Daflon)Drug

    Diosmin / Hesperidin (Daflon) 500 mg will be taken once daily for 12 weeks with the standard treatment

  • no intervention (control group)Other

    this group will receive no intervention (only the standard treatment)

Study groups in NCT07293767
Study groupRoleWhat they receive
Silymarin groupExperimentalthis group of patients will receive silymarin (LEGALON) 140 mg three times daily with the standard treatment
Receives: Drug: Silymarin (LEGALON)
Diosmin/hisperedin groupExperimentalthis group will receive hesperidin/diosmin (daflon) 500 once daily for 12 weeks with the standard treatment
Receives: Drug: Diosmin / Hesperidin (Daflon)
Standard care groupActive comparatorparticipants will receive standard treatment only
Receives: Other: no intervention (control group)

What is being measured

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

  1. pain assessment through Fibromyalgia impact questionnaire (FIQ)

    Change in Fibromyalgia impact questionnaire (FIQ) score will be assessed by the end of the study, the score ranges from 0 to 100 higher score means worse condition

    Measured: 4 months

Secondary outcomes (5)
  1. Erythrocyte sedimentation rate (ESR)

    ESR will be measured at baseline and after four months of treatment

    Measured: 4 months

  2. C-reactive protein level (CRP)

    CRP will be measured at baseline and after four months of treatment

    Measured: 4 months

  3. Health-related quality-of-life through Short Form 12 health survey SF-12

    quality of life will be assessed through Short Form 12 health survey SF-12 (Questionnaire of health) at baseline and after 4 months the score ranges from 0 to 100 higher scores indicate better health

    Measured: 4 months

  4. pain assessment through visual analogue scale (VAS)

    visual analogue scale (VAS) score will be assessed at baseline and after four months of treatment, the score ranges from 0 to 10 cm higher score means worse condition

    Measured: 4 months

  5. laboratory evaluation of interleukin- 8 (IL-8) level

    serum IL8 concentration will be measured at baseline and after four months of treatment.

    Measured: 4 months

Timeline

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

  1. First posted19 Dec 2025
  2. Study start16 Nov 2024
  3. Primary completion15 Jan 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Group I: 30 patients will receive their standard treatment of fibromyalgia for four months. Group II: 30 patients will receive 500 mg of diosmin/ hesperidine combination under the trade name of daflon with their standard treatment of fibromyalgia for four months. Group III: 30 patients will receive 140 mg of silymarin three times daily under the trade name of Legalon with their standard treatment for four months.
Masking
None (open label)
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07293767
Sponsor's protocol ID
FM
Acronym
SHD-FM
Status last verified
Dec 2025
First submitted
25 Nov 2025
Last updated
19 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Silymarin (LEGALON) and Diosmin / Hesperidin (Daflon) in people with Fibromyalgia (FM), run by Ain Shams University at 1 site in Egypt.

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: looking for participants now, as of the sponsor's last update on 19 Dec 2025. 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 Egypt. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact menna s teaching assistant of clinical pharmacy/ master's student (01064897439, mssalama@msa.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

pain assessment through Fibromyalgia impact questionnaire (FIQ) (time frame: 4 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 19 Dec 2025.

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