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The effect of ginger consumption in patients with multiple sclerosis

The effect of ginger consumption on serum levels of neurofilament light polypeptide, matrix metalloproteinase-9, interleukin-17, nitric oxide metabolites, and differential leukocyte count and score of disability status, quality of life, and gastrointestinal symptoms in patients with multiple sclerosis: a double-blind randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180818040827N3
Enrollment
50
Registered
2021-10-06
Start date
2021-10-22
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple sclerosis. Multiple sclerosis

Interventions

Intervention 1: Intervention group: 500 mg ginger supplements three times a day for 12 weeks. Intervention 2: Control group: 500 mg corn supplements (placebo) three times a day for 12 weeks.

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Having relapsing-remitting multiple sclerosis according to the 2017 revisions of the McDonald diagnostic criteria Age between 18-50 years Non-menopausal women Disability status score of less than or equal to 4.5 based on Expanded Disability Status Scale No multiple sclerosis attack or corticosteroid therapy for at least 30 days No change in multiple sclerosis medications for at least 6 months Ability and willingness to participate in the study

Exclusion criteria

Exclusion criteria: Having other serious diseases such as other autoimmune disorders or cancers Pregnancy Multiple sclerosis attack or corticosteroid therapy during the intervention Change in multiple sclerosis medications during the intervention Allergic reactions to ginger or placebo supplements Consumption of less than 90% of ginger or placebo supplements

Design outcomes

Primary

MeasureTime frame
Score of disability status. Timepoint: Before and after the intervention. Method of measurement: Expanded Disability Status Scale.;Serum levels of interleukin-17. Timepoint: Before and after the intervention. Method of measurement: Assay kit.;Serum levels of nitric oxide metabolites. Timepoint: Before and after the intervention. Method of measurement: Assay kit.

Secondary

MeasureTime frame
Serum levels of neurofilament light polypeptide. Timepoint: Before and after the intervention. Method of measurement: Assay kit.;Serum levels of matrix metalloproteinase-9. Timepoint: Before and after the intervention. Method of measurement: Assay kit.;Differential leukocyte count. Timepoint: Before and after the intervention. Method of measurement: Cell counter machine.;Score of quality of life. Timepoint: Before and after the intervention. Method of measurement: Multiple Sclerosis Impact Scale.;Score of gastrointestinal symptoms. Timepoint: Before and after the intervention. Method of measurement: Visual Analogue Scale.;Hematological indices. Timepoint: Before and after the intervention. Method of measurement: Cell counter machine.;Body mass index. Timepoint: Before and after the intervention. Method of measurement: Weighing scale and measuring tape.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Amani

Esfahan University of Medical Sciences

r_amani@nutr.mui.ac.ir+98 31 3668 1378

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 10, 2026