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CompletedNCT04395547Updated Dec 23, 2022

Safety and Efficacy of JointAlive™ on the Knee-joint Function in Adults With Knee Arthritis

An interventional study of JointAlive™ and Placebo in Osteo Arthritis Knee, sponsored by Chenland Nutritionals Inc.. Completed at 1 site in Canada. Open to participants aged 40 Years to 75 Years. Per ClinicalTrials.gov, last updated 2022-12-23.

Sponsored by Chenland Nutritionals Inc. · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
72
Allocation
Randomized
Ages
40 Years to 75 Years
Sex
All
01

Study summary

Osteoarthritis (OA) is a joint disorder caused by wear and tear on the joint over time; as a result, the protective cartilage of the bone in the joint gradually wears down. The lifetime risk of developing OA in the knee, with symptoms such as pain, aching, and stiffness, is 40% in men and 47% in women. It is estimated that approximately 19% of Americans aged 45 and older are affected by knee OA. Knee OA accounts for 83% of the global burden caused by all OA types. Pain and stiffness in knees, a large weight-bearing joint, often leads to disability, which interferes with daily life activities and demands expensive medical treatments or care. Due to the limitations of current OA treatment methods, there is an increasing demand for effective and safer alternatives, such as natural health products with pain-relieving potential. The investigational product, JointAlive™, is a supplement designed to alleviate knee OA symptoms and to improve knee functionality. The present study will investigate the safety and efficacy of JointAlive™ in reducing knee OA symptoms and improving joint functionality in an otherwise healthy adult population with mild to moderate knee OA. JointAlive™ is a proprietary blend of Epimedium brevicornum Maxim leaves, Dioscorea nipponica Makino rhizome, Salvia miltoiorrhiza Bunge root and rhizome extracts

Read the detailed description

Osteoarthritis (OA) is a joint disorder caused by wear and tear on the joint over time; as a result, the protective cartilage of the bone in the joint gradually wears down. The lifetime risk of developing OA in the knee, with symptoms such as pain, aching, and stiffness, is 40% in men and 47% in women. It is estimated that approximately 19% of Americans aged 45 and older are affected by knee OA. Knee OA accounts for 83% of the global burden caused by all OA types. Pain and stiffness in knees, a large weight-bearing joint, often leads to disability, which interferes with daily life activities and demands expensive medical treatments or care. Losina et al. reported that in the United States, the average lifetime costs for symptomatic knee OA management is $12,400 USD, but the cost can be higher with knee surgeries for advanced OA. The economic burden is expected to continue increasing in the near future due to the aging population and increasing prevalence of obesity in many developed countries.

Although the exact etiology of OA is unknown, many risk factors are associated with the development of knee OA, such as obesity, repetitive use of joints, age, and previous knee injury or surgery. Multiple studies have shown a positive association between pro-inflammatory cytokines (e.g. tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and IL-6) and OA development. Cytokine-induced nuclear factor-κB (NF-κB) activation can stimulate articular chondrocyte catabolism and extracellular matrix degradation, leading to the breakdown of articular cartilage. The severity of cartilage disintegration and osteophyte (a bony outgrowth) formation can be identified radiographically and used for the Kellgren-Lawrence (KL) grading scheme. A KL score of one (doubtful narrowing of the joint space with possible osteophyte formation) is considered possible OA, while a score of two (possible narrowing of joint space with definite osteophyte formation) or three (definite narrowing of joint space and moderate osteophyte formation) is considered as a definite/mild OA.

It is crucial to treat OA early, before it develops into more severe cases and causes mobility disability. The first step of OA treatment is exercise and/or physiotherapy, which has demonstrated long-term benefits but often difficult to maintain compliance. Once the pain is difficult to manage, over-the-counter medicines such as Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) are introduced to provide relief. NSAIDs are effective in reducing pain, however, long-term usage requires medical supervision. Chronic NSAID use is associated with high incidence of adverse events such as upper gastrointestinal tract problems, kidney and liver injury, hypertension, and congestive heart failure. When the abovementioned treatments are ineffective, intra-articular injections of hyaluronic acid, cortisol, or platelet rich plasma are applied and proven effective, but they can be costly and may cause reactive flares or infections at the injection site. Surgery serves as last resort; it is a successful treatment for advanced OA, but it is invasive and may increase risks of infection, bleeding, and deep vein thrombosis. Given the limitations of current OA treatment methods, there is an increasing demand for effective and safer alternatives, such as natural health products with pain-relieving potential.

The investigational product, JointAlive™, is a supplement designed to alleviate knee OA symptoms and to improve knee functionality. JointAlive™ contains extract from flowering plants that are endemic to China.The main bioactive component is icariin; a flavonoid glycoside demonstrating various antioxidant and anti-inflammatory benefits. Numerous in vitro cell culture studies showed that icariin has the potential to suppress inflammatory pathways involved in OA. In rodent OA models, joint injection of icariin for 32 and 84 days was found to protect the articular cartilage from degeneration.

The present study will investigate the safety and efficacy of JointAlive™ in reducing knee OA symptoms and improving joint functionality in an otherwise healthy adult population with mild to moderate knee OA. Based on the previous studies conducted on the ingredients of this investigational product and their previous application in OA, participants identifying mild or moderate OA in a target knee will be investigated in this study. As OA is a secondary complication in sports injuries as well as a primary development during aging, an age range between 40-75 years will be considered for enrolment. The Kellgren-Lawrence grading scale will be used to confirm OA. As well, BMI cut offs between 18.5 and 29.9 kg/m2 will be considered to excluded those with complications due to obesity and the associated increase in concomitant medication use. To allow for pain relief, as this study involves a placebo group, a rescue medication will be provided. However, in order to ensure that the capture of pain in the target knee is unbiased, participants will be required to abstain from the rescue medication use for 48 hours prior to their clinic visits. Confounders due to medical history and concomitant medications will be ensured by several targeted exclusion criteria with the intent of decreasing potential confounders of the study results.

02

Conditions studied

  • Osteo Arthritis Knee
03

In context

Arthritis

3,554 studies on the registry are indexed under Arthritis; 317 are open to participants now.

This study's enrollment of 72 is below the median of 90 across 2,377 interventional studies indexed under Arthritis.

Browse Arthritis studies →

Lead sponsor

Chenland Nutritionals Inc. is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Males and females between 40 and 75 years of age, inclusive
  2. BMI between 18.5 to 29.9 kg/m2, inclusive

  3. Female participant is not of child-bearing potential, defined as females who have undergone a sterilization procedure (e.g. hysterectomy, bilateral oophorectomy, bilateral tubal ligation, complete endometrial ablation) or have been post-menopausal for at least 1 year prior to screening Or,

    Females of child-bearing potential must have a negative baseline urine pregnancy test and agree to use a medically approved method of birth control for the duration of the study. All hormonal birth control must have been in use for a minimum of three months. Acceptable methods of birth control include:

    • Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo-Provera, Lunelle), or hormone implant (Norplant System)
    • Double-barrier method
    • Intrauterine devices
    • Non-heterosexual lifestyle or agrees to use contraception if planning on changing to heterosexual partner(s)
    • Vasectomy of partner at least 6 months prior to screening
  4. Self-reported pain or swelling in target knee
  5. The diagnosis of mild to moderate osteoarthritis as confirmed by the Qualified Investigator using qualifiers based on physical exam, medical history and x-ray report qualified as mild to moderate by the radiologist
  6. Agrees to refrain from taking any pain relievers during the study, except acetaminophen as a rescue medication specified by the study site
  7. Agrees to refrain from taking rescue medication for 48 hours prior to study visits
  8. Agrees to maintain current diet and current exercise routine throughout the study
  9. Willingness to complete questionnaires, records, and diaries associated with the study and to complete all clinic visits
  10. Provided voluntary, written, informed consent to participate in the study
  11. Healthy as determined by medical history, laboratory results, and physical exam as assessed by the Qualified Investigator (QI)

Exclusion criteria

Exclusion Criteria:

  1. Allergy, sensitivity, or intolerance to the investigational product's active or inactive ingredients
  2. Allergy to rescue medication
  3. Women who are pregnant, breast feeding, or planning to become pregnant during the study
  4. Clinically significant abnormal laboratory results at baseline as assessed by the QI
  5. Individuals who are unable to give informed consent
  6. Injury in the target knee within the past 3 months
  7. Intraarticular injections in the target knee within the past 6 months, or plan to have intraarticular injections during the study
  8. Individuals with knee joint diseases, such as rheumatoid arthritis, gouty arthritis, septic arthritis or any other infective arthritis
  9. Self-reported history of gout or pseudo gout within the past 6 months
  10. Skin defects (e.g. skin and soft tissue infections that cause necrosis of the skin, or post-burn contractures) and ulcers around the affected knee joint, as assessed by the QI
  11. History of knee surgery or replacement in the target knee, or any non-knee surgical procedures that may impact the study outcomes as assessed by the QI
  12. Individuals with muscle or skeletal disorders as assessed by the QI
  13. Unstable metabolic disease or chronic diseases as assessed by the QI
  14. In a state of acute exacerbation or seizure of chronic disease
  15. Type I or Type II diabetes
  16. History of or current diagnosis with severe cardiopulmonary, kidney and/or liver dysfunctions, with the exception of history of kidney stones in participants who are symptom free for 6 months
  17. Self-reported confirmation of current or pre-existing thyroid condition. Treatment on a stable dose of medication for at least 3 months will be considered by the QI
  18. Current or history of any significant diseases of the gastrointestinal tract including diarrhea or dysentery as assessed by the QI
  19. Significant cardiovascular event in the past 6 months. Participants with no significant cardiovascular event on stable medication may be included after assessment by the QI on a case-by-case basis
  20. Self-reported confirmation of medical or neuropsychological condition and/or cognitive impairment that, in the QI's opinion, could interfere with study participation
  21. Cancer, except skin basal cell carcinoma completely excised with no chemotherapy or radiation with a follow up that is negative. Volunteers with cancer in full remission for more than five years after diagnosis are acceptable
  22. Verbal confirmation of blood/bleeding disorders as assessed by the QI
  23. Individuals with an acute infectious disease, autoimmune disease or are immune-compromised
  24. Self-reported confirmation of a HIV-, Hepatitis B- and/or C-positive diagnosis
  25. Current use of prescribed medications listed above
  26. Current use of over-the-counter medications, supplements, foods and/or drinks listed above
  27. Use of medical cannabinoid products
  28. Chronic use of cannabinoid products (>2 times/week) and is unwilling to stop use for the duration of the study. Occasional use to be assessed by the QI on a case-by-case basis
  29. Alcohol or drug abuse within the last 12 months
  30. High alcohol intake (average of >2 standard drinks per day)
  31. Blood donation 30 days prior to screening, during the study, or a planned donation within 30 days of the last study visit
  32. Participation in other clinical research studies 30 days prior to screening
  33. Any other condition, that, in the opinion of the QI, may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant

Participants on the following concurrent prescribed medications and/or treatments will be excluded during enrollment unless they have been taken off these therapies by their family physician. In the latter event, the frequency and route of administration of use and/or dosage may be considered by the QI on a case-by-case basis prior to recommending an appropriate washout or their enrollment in the study.

  1. Oral NSAIDs or topical application on the target knee
  2. Narcotics
  3. Oral corticosteroids or topical application on the target knee
  4. Oral analgesics except acetaminophen as a rescue medication or topical application on the target knee
  5. Digoxin
  6. Anti-hypertensive drugs
  7. Anticoagulants or antiplatelet drugs
  8. Medications used for OA treatment
  9. Diazepam
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
72 participants (actual)

Study arms

  • Placebo comparator
    Placebo

    Dietary Supplement: Placebo

  • Experimental
    JointAlive™

    Dietary Supplement: JointAlive™

Interventions

  • Dietary supplementJointAlive™

    Combination herbal extract

  • Dietary supplementPlacebo

    Combination placebo product

06

What researchers measure

Primary outcomes

  1. Change in knee joint function: Pain

    This will be determined by change in pain of the identified knee joint from baseline to 12-week post-supplementation between JointAlive™ and placebo, as assessed by Western Ontario McMaster Universities Osteoarthritis Index (WOMAC) pain and stiffness scores. Questions are scored on a scale of 0-4, which correspond to: None (0), Mild (1), Moderate (2), Severe (3), and Extreme (4). The scores for each subscale are summed up, with a possible score range of 0-20 for Pain. The lowest number represents no pain while the highest number represent extreme pain or stiffness. These are then converted to the Knee injury and Osteoarthritis Outcomes Score (KOOS) pain scores. KOOS scoring system ranges from 1-100, with 0 representing no pain and 100 being extreme pain.

    Time frame: 12 weeks

  2. Change in knee joint function: Stiffness

    This will be determined by change in stiffness of the identified knee joint from baseline to 12-week post-supplementation between JointAlive™ and placebo, as assessed by Western Ontario McMaster Universities Osteoarthritis Index (WOMAC) pain and stiffness scores. Questions are scored on a scale of 0-4, which correspond to: None (0), Mild (1), Moderate (2), Severe (3), and Extreme (4). The scores for each subscale are summed up, with a possible 0-8 for Stiffness. The lowest number represents no pain or stiffness while the highest number represent extreme pain or stiffness. These are then converted to the Knee injury and Osteoarthritis Outcomes Score (KOOS) pain scores. KOOS scoring system ranges from 1-100, with 0 representing no stiffness and 100 being extreme stiffness.

    Time frame: 12 weeks

Secondary outcomes

  1. Change in Pain

    Change in pain of the identified knee joint from baseline to 6-week post-supplementation between JointAlive™ and placebo, as assessed by Western Ontario McMaster Universities Osteoarthritis Index (WOMAC) pain and stiffness scores. Questions are scored on a scale of 0-4, which correspond to: None (0), Mild (1), Moderate (2), Severe (3), and Extreme (4). The scores for each subscale are summed up, with a possible score range of 0-20 for Pain. The lowest number represents no pain while the highest number represent extreme pain or stiffness. These are then converted to the Knee injury and Osteoarthritis Outcomes Score (KOOS) pain scores. KOOS scoring system ranges from 1-100, with 0 representing no pain and 100 being extreme pain.

    Time frame: 6 weeks

  2. Change in Stiffness

    Change in stiffness of the identified knee joint from baseline to 6-week post-supplementation between JointAlive™ and placebo, as assessed by Western Ontario McMaster Universities Osteoarthritis Index (WOMAC) pain and stiffness scores. Questions are scored on a scale of 0-4, which correspond to: None (0), Mild (1), Moderate (2), Severe (3), and Extreme (4). The scores for each subscale are summed up, with a possible 0-8 for Stiffness. The lowest number represents no pain or stiffness while the highest number represent extreme pain or stiffness. These are then converted to the Knee injury and Osteoarthritis Outcomes Score (KOOS) pain scores. KOOS scoring system ranges from 1-100, with 0 representing no stiffness and 100 being extreme stiffness.

    Time frame: 6 weeks

  3. Knee OA symptoms as assessed by KOOS symptoms score

    KOOS Scores range from 0 to 100. A score of 0 indicates the worst possible knee symptoms and 100 indicates no knee symptoms.

    Time frame: 6-12 weeks

  4. Daily physical function as assessed by KOOS in function daily living score

    The Scoring system ranges from 0 to 100, with 0 representing extreme problems and 100 representing no problems

    Time frame: 6-12 weeks

  5. Physical function in sports and recreational activities as assessed by KOOS function in sports and recreational activities score

    The Scoring system ranges from 0 to 100, with 0 representing extreme problems with physical functions and 100 representing no problems

    Time frame: 6-12 weeks

  6. Current pain as assessed by Pain Visual Analogue Scale (VAS) scores

    The Pain VAS questionnaire is a unidimensional measure of pain intensity. With the use of a ruler, the score is determined by measuring the distance (mm) on the 10-cm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-100 depending on pain intensity. A score of 0 represents no pain while a score of 100 represents extreme pain.

    Time frame: 6-12 weeks

  7. Quality of life as assessed by Short Form 36 (SF-36) Questionnaire and KOOS quality of life score

    The Scoring system ranges from 0 to 100, with 0 representing poorest quality of life and 100 representing no problems

    Time frame: 6-12 weeks

  8. Knee joint range of motion (flexion and extension) as assessed by a knee goniometer

    Time frame: 6-12 weeks

  9. Serum level of C reactive protein (CRP)

    Time frame: 6-12 weeks

  10. Use of acetaminophen as a rescue medication as assessed by study diary

    Time frame: 6-12 weeks

Other outcomes

  1. Incidence of pre-emergent and post-emergent adverse events

    Time frame: 12 weeks

  2. Blood pressure (BP)

    Diastolic and systolic blood pressure (BP) after 6 and 12 weeks of supplementation with JointAlive™

    Time frame: 12 weeks

  3. Heart Rate

    Heart rate (HR) after 6 and 12 weeks of supplementation with JointAlive™

    Time frame: 12 weeks

  4. Change alanine aminotransferase (ALT) after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  5. Change aspartate aminotransferase (AST) after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  6. Change alkaline phosphatase (ALP), after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  7. Change in total bilirubin after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  8. Change in total creatinine after 12 weeks of supplementation with JointAlive™ compared to placebo

    Time frame: 12 weeks

  9. Change in electrolytes (Na+, K+, Cl-) after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  10. Change in estimated glomerular filtration rate (eGFR) after 12 weeks of supplementation with JointAlive™ compared to placebo

    Time frame: 12 weeks

  11. Change in white blood cell (WBC) count after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  12. Change in neutrophils after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  13. Change in lymphocytes after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  14. Change in monocytes after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  15. Change in eosinophils after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  16. Change in basophils after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  17. Change in red blood cell (RBC) count after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  18. Change in hemoglobin after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  19. Change in hematocrit after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  20. Change in platelet count after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  21. Change in mean corpuscular volume (MCV) after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  22. Change in mean corpuscular hemoglobin (MCH) after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  23. Change in mean corpuscular hemoglobin concentration (MCHC) after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  24. Change in red cell distribution width (RDW) after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

  25. Change in mean platelet volume (MPV) after 12 weeks of supplementation with JointAlive™ compared to placebo.

    Time frame: 12 weeks

07

Study locations

1 site
  • KGK Science Inc
    London, Ontario N6A 5R8, Canada
08

References and documents

Publications

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Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 23, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04395547
Lead sponsor
Chenland Nutritionals Inc.
Collaborators
KGK Science Inc.
Responsible party
Sponsor
First posted
May 20, 2020
Start date
Jun 15, 2020
Primary completion
May 27, 2022
Completion
May 27, 2022
Last update
Dec 23, 2022

Study contacts

David Crowley, MD
principal investigator · KGK Science Inc.

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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