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The effect of ginger supplementation on pain and inflammatory factors

The effect of ginger supplementation on pain and some pro-inflammatory cytokins in knee osteoarthritis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201112078321N1
Enrollment
100
Registered
2012-05-24
Start date
2011-07-06
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

osteoarthritis. Primary generalized (osteo)arthrosis

Interventions

Intervention 1: Ginger group took the capsules 500 mg (ginger powder as drug) 2 times a day. Duration of this intervention was 3 months. Intervention 2: Placebo group took the capsules 500 mg (starch
Treatment - Drugs
Placebo
Ginger group took the capsules 500 mg (ginger powder as drug) 2 times a day. Duration of this intervention was 3 months.
Placebo group took the capsules 500 mg (starch powder) 2 times a day. Duration of this intervention was 3 months.

Sponsors

Yazd University of Medical Scieces
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: to complete the inform consent; the presence of medium knee pain between 40mm and 70 mm on a 100-mm visual analog scale (VAS) during the preceding 24 hours; the age between 50 and 70 years; absence of following conditions: inflammatory disease, metabolic disorder such as diabetes, dementia, rheumatoid arthritis, fibromyalgia, gout, cancer or other serious disease, signs or history of liver or kidney failure, asthma requiring treatment with steroids; treatment with oral corticosteroids within the prior 4 weeks; intraarticular knee depo-corticosteroids within the previous 3 months; prior treatment with immunosuppressive drugs such as penicillamine; arthroscopy of the target joint within the previous yea; significant injury to the target joint within the previous 6 months; fever >38 degree C at screening; allergy to ginger. Exclusion criteria: serious complications; consumption of vitamin-mineral supplements or other nutritional supplements; consumption of analgesics.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before the intervention and 12 weeks after the end of treatment. Method of measurement: visual analoge scale.

Secondary

MeasureTime frame
Some pro-inflammatory cytokins. Timepoint: before the intervention and after 12 weeks. Method of measurement: ELISA kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Naderi

Shahid Sadooghi university of medical sciences

zhr_naderi@yahoo.com ; zhr_naderi@ssu.ac.ir+98 35 1836 7668

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026