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Effects of Anthriscus Sylvestris Leaves on Mild Knee Osteoarthritis

P

Pusan National University

Status

Completed

Conditions

Osteoarthritis
Articular Cartilage
Functional Food

Treatments

Dietary Supplement: microcrystalline cellulose
Dietary Supplement: Aqueous extract of A. sylvestris leaves

Study type

Interventional

Funder types

Other

Identifiers

NCT06535204
H-1905-043-079

Details and patient eligibility

About

Osteoarthritis (OA) is a common degenerative joint disorder that causes pain, stiffness, and functional impairment. Current treatments for OA are limited to symptom relief and have potential side effects. Anthriscus sylvestris leaves are a natural remedy that has been shown to have anti-inflammatory and cartilage-protective effects in animal models of OA.

Full description

Osteoarthritis (OA) is a common degenerative joint disorder that causes pain, stiffness, and functional impairment. Current treatments for OA are limited to symptom relief and have potential side effects. Anthriscus sylvestris leaves are a natural remedy that has been shown to have anti-inflammatory and cartilage-protective effects in animal models of OA. A randomized, double-blind, placebo-controlled trial was conducted with 100 participants aged 40 to 75 with Kellgren & Lawrence grade 1 or 2 knee OA. Participants were assigned to receive either 500 mg of Anthriscus sylvestris leaves extract or placebo daily for 12 weeks. The primary outcome was the change in the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score from baseline to week 12. Secondary outcomes included the changes in visual analogue scale (VAS) for pain, C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR) from baseline to week 12. The Anthriscus sylvestris leaves extract group showed a significant improvement in the total WOMAC score, as well as the pain, stiffness, and physical function sub-scores, compared with the placebo group after 12 weeks of treatment. The Anthriscus sylvestris leaves extract group also showed a significant reduction in VAS and CRP, but not in ESR, compared with the placebo group. No adverse events or safety concerns were reported in either group. Anthriscus sylvestris leaves extract enhanced joint and cartilage health in humans with mild OA symptoms, as indicated by the reduction in WOMAC, VAS, and CRP. The extract was also safe and well-tolerated. Anthriscus sylvestris leaves extract may be a promising natural alternative for the management and prevention of OA.

Enrollment

100 patients

Sex

All

Ages

40 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults aged 40 to 75 years, regardless of gender
  • Individuals with a Visual Analogue Scale (VAS) score of 3/10 or higher
  • Individuals with a Kellgren & Lawrence grading scale of grade 1 or 2, determined by 'Both Knee Joint AP/LAT' radiographs
  • Individuals who have had a washout period of at least 4 weeks for arthritis- related medications or health supplements
  • Individuals capable of normal physical activity who have voluntarily provided written informed consent to participate in this study

Exclusion criteria

  • Individuals with a history of fractures within the past year
  • Individuals with osteophytes around the joints, irregular joint surfaces, or subchondral bone cysts, indicating moderate arthritis
  • Individuals currently undergoing treatment for a diagnosed thyroid disorder
  • Individuals with kidney disease or serum creatinine levels of 1.4 mg/dL or higher
  • Individuals with proteinuria of 2+ or higher
  • Individuals with liver disease or AST or ALT levels of 100 IU/L or higher
  • Individuals with uncontrolled hypertension or heart conditions such as angina or myocardial infarction
  • Individuals taking medication for psychiatric disorders, except for intermittent medication for sleep disorders
  • Individuals who have taken herbal or medicinal decoctions within the past two months
  • Individuals who have received other investigational drugs within the past four weeks
  • Individuals who need to continuously take medication that may affect the outcome of the study
  • Individuals with a history of gastrointestinal resection surgery (excluding appendectomy)
  • Pregnant or breastfeeding women
  • Individuals with alcoholism or those who drink more than four times per week regularly
  • Individuals with hypersensitivity to the test food or its ingredients
  • Individuals who may be uncooperative or deemed incapable of completing the study by the investigator
  • Individuals with arthritis due to specific factors other than degeneration, as determined by the principal investigator

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

100 participants in 2 patient groups, including a placebo group

Experimental Group
Experimental group
Description:
The intervention group consumed the test food twice daily (400 mg in the morning and 400 mg in the evening, each time as one hard capsule), 30 minutes after eating, with water. The administration period lasted 12 weeks for each participant. The test food is named Aqueous extract of A. sylvestris leaves. The ingredients and their contents are as follows: Aqueous extract of A. sylvestris leaves 62.5%, Microcrystalline Cellulose 35.5%, Silicon Dioxide 1.0%, Magnesium Stearate 1.0%. The dosage form is a hard capsule, with a content weight of 400 mg per capsule.
Treatment:
Dietary Supplement: Aqueous extract of A. sylvestris leaves
Control Group
Placebo Comparator group
Description:
The Control group consumed the test food twice daily (400 mg in the morning and 400 mg in the evening, each time as one hard capsule), 30 minutes after eating, with water. The administration period lasted 12 weeks for each participant. The test food is named Microcrystalline Cellulose. The ingredients and their contents are as follows: Microcrystalline Cellulose 98%, Silicon dioxide 1.0%, Magnesium stearate 1.0%. The dosage form is a hard capsule, with a content weight of 400 mg per capsule.
Treatment:
Dietary Supplement: microcrystalline cellulose

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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