Effect of Probiotics in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
NCT ID: NCT04741841
Last Updated: 2021-10-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
74 participants
INTERVENTIONAL
2020-03-30
2021-06-30
Brief Summary
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Detailed Description
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The exact cause of the ME/CFS is presently unknown however a history of viral infection is common among ME/CFS patients. Prolonged post viral fatigue can develop into a chronic illness and ME/CFS. Current research strongly suggests involvement of gastrointestinal tract and gut microflora disturbances in the pathogenesis with strong evidence supporting the role of imbalance of gut microflora, damaged gut barrier functions and dysfunctional immune responses. There are some features shared with gastrointestinal conditions like irritable bowel syndrome (IBS). GutMagnific™ is an evidence-based probiotic food supplement, scientifically designed to be effective in correcting imbalances of the gut microflora, repairing a damaged gut barrier and reducing inflammation. The strain combination in GutMagnific™ has been carefully designed for its efficacy in IBS and therefore it can be reasonably expected to be also effective in ME/CFS.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Placebo
The placebo product is identical to active product in taste and appearance but without probiotic
Placebo
Vegan capsules identical to active product in taste and appearance but without probiotic
Treatment high dose
High dose GutMagnific™
GutMagnific™ H.
Vegan Capsules with active product, GutMagnific™ high dose
Treatment low dose
Low dose GutMagnific™
GutMagnific™ L.
Vegan Capsules with active product, GutMagnific™ low dose
Interventions
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GutMagnific™ H.
Vegan Capsules with active product, GutMagnific™ high dose
GutMagnific™ L.
Vegan Capsules with active product, GutMagnific™ low dose
Placebo
Vegan capsules identical to active product in taste and appearance but without probiotic
Eligibility Criteria
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Inclusion Criteria
* Gastrointestinal complications similar to IBS
Exclusion Criteria
* Consumption of other probiotic products during the trial
18 Years
ALL
No
Sponsors
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Karolinska Institutet
OTHER
ImmuneBiotech Medical Sweden AB
INDUSTRY
Responsible Party
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Principal Investigators
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Per Julin, MD/PhD
Role: PRINCIPAL_INVESTIGATOR
Karolinska Institutet
Locations
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Neurological Rehabilitation Clinic in Stora Sköndal
Stockholm, , Sweden
Countries
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Other Identifiers
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GM_ME/CFS_2020SE
Identifier Type: -
Identifier Source: org_study_id