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New supplement shows promise for fibromyalgia sufferers

NCT ID NCT07495943

Symptom relief Sponsor: Haydarpasa Numune Training and Research Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a supplement called FibroThol (containing 2-Aticyto Complex and D-ribose) can help reduce pain and other symptoms in people with fibromyalgia. About 200 adults aged 18 to 65 who have had fibromyalgia for at least a year and are already on standard medications will take either the supplement or a placebo for 4 weeks. The goal is to see if adding this supplement provides extra relief beyond current treatments.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

May 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adults aged 18 to 65 years * Diagnosis of fibromyalgia syndrome according to the 2016 ACR criteria * Followed in a physical medicine and rehabilitation outpatient clinic for at least 1 year * Receiving pregabalin and/or duloxetine treatment for at least 3 months * Able to live independently in the community * Literate and able to record symptoms and responses * No cognitive dysfunction that would interfere with answering study questions * Able and willing to provide informed consent Exclusion Criteria: * Rheumatologic disease * Renal failure * Hepatic failure * Cardiovascular disease * Hypoglycemia or diabetes mellitus * Any neurologic disease (such as stroke, spinal cord injury, multiple sclerosis, or Parkinson's disease) * Known allergy or hypersensitivity to any active or excipient component of the study syrup * Use of any other dietary supplement or nutritional support product during the study period * Pregnancy or lactation * Active malignancy * Active infection * Severe psychiatric disease that may interfere with study participation or assessment * Refusal to participate or inability to provide informed consent

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Conditions

The condition(s) this trial relates to.

anxiety disorder Depression fibromyalgia insomnia Pain

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Fibromyalgia Fibromyalgia syndrome

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    5 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Erenkoy Physical Therapy and Rehabilitation Hospital, Department of Physical Medicine and Rehabilitation

    Istanbul, 34732, Turkey (Türkiye)

  • University of Health Sciences, Basaksehir Cam and Sakura City Hospital, Department of Physical Medicine and Rehabilitation

    Istanbul, 34480, Turkey (Türkiye)

  • University of Health Sciences, Fatih Sultan Mehmet Training and Research Hospital, Department of Physical Medicine and Rehabilitation

    Istanbul, 34752, Turkey (Türkiye)

  • University of Health Sciences, Haydarpasa Numune Training and Research Hospital, Department of Physical Medicine and Rehabilitation

    Istanbul, Istanbul, 34662, Turkey (Türkiye)

  • University of Health Sciences, Sultan Abdulhamid Han Training and Research Hospital, Department of Physical Medicine and Rehabilitation

    Istanbul, 34668, Turkey (Türkiye)

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