Comarum Palustre in Knee Osteoarthritis and Diabetes

Sponsor
Federal State Budgetary Scientific Institution, Research Institute of Fundamental and Clinical Immunology (Other)
Overall Status
Completed
CT.gov ID
NCT03530930
Collaborator
(none)
15
1
1
4.9
3.1

Study Details

Study Description

Brief Summary

The study evaluates analgesic, antiinflammatory and metabolic effects of Comarum palustre in patients with knee osteoarthritis (OA) and diabetes mellitus. Patients with osteoarthritis will receive Comarum palustre together with conventional treatment of osteoarthritis and diabetes.

Condition or Disease Intervention/Treatment Phase
  • Drug: Comarum Palustre
Phase 4

Detailed Description

Comarum palustre have been shown to exert analgesic properties in patients with knee osteoarthritis not responding to diclofenac. In animal models comarum palustre showed anti-inflammatory, immunomodulatory, analgesic, antioxidant, antihistamine, and membrane-stabilizing effects. Thus, pleiotropic properties of Comarum Palustre may provide a rationale for this use in patients having both osteoarthritis and diabetes mellitus. In this group of patients Comarum Palustre may not only relieve OA-related pain but reduce systemic inflammation, decrease progression of atherosclerosis and diabetes complications.

Study Design

Study Type:
Interventional
Actual Enrollment :
15 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Analgesic, Antiinflammatory and Metabolic Effects of Comarum Palustre in Patients With Osteoarthritis and Diabetes Mellitus
Actual Study Start Date :
Jun 29, 2018
Actual Primary Completion Date :
Nov 25, 2018
Actual Study Completion Date :
Nov 25, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Comarum Palustre

Patients taking Comarum Palustre together with conventional treatment for osteoarthritis

Drug: Comarum Palustre
Comarum Palustre tablets 500 mg BID, 1 month
Other Names:
  • Potentilla palustris
  • Outcome Measures

    Primary Outcome Measures

    1. Change From Baseline in Visual Analogue Scale for Pain [Baseline, 4 weeks]

      The Visual Analogue Scale for Pain varies from 0 to 10 cm. Higher values represent worse outcomes.

    Secondary Outcome Measures

    1. Knee injury and Osteoarthritis Outcome Score (KOOS) - subscale Pain [Baseline, 4 weeks]

      KOOS Pain consists of 9 items, which are answered on a 4-point likert scale (0=no problems, 4=extreme problems). Scores are transformed to a 0-100 scale, with zero representing extreme knee problems and 100 representing no knee problems.

    2. Knee injury and Osteoarthritis Outcome Score (KOOS) - subscale Activities of daily living (ADL) [Baseline, 4 weeks]

      KOOS ADL consists of 17 items, which are answered on a 4-point likert scale (0=no problems, 4=extreme problems). Scores are transformed to a 0-100 scale, with zero representing extreme knee problems and 100 representing no knee problems.

    3. Knee injury and Osteoarthritis Outcome Score (KOOS) - subscale Symptoms [Baseline, 4 weeks]

      KOOS Symptoms consists of 7 items, which are answered on a 4-point likert scale (0=no problems, 4=extreme problems). Scores are transformed to a 0-100 scale, with zero representing extreme knee problems and 100 representing no knee problems.

    4. Quality of life with the The Short Form (36) Health Survey score [Baseline, 4 weeks]

      The Short Form (36) Health Survey is a 36-item, patient-reported survey of patient health. The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section.Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.

    5. Intermittent and Constant Osteoarthritis Pain self-report questionnaire [Baseline, 4 weeks]

      Pain measure: Scale range 0-100 with higher scores indicating worse pain

    6. Changes in serum levels of aggrecan [Baseline, 4 weeks]

      serum levels of aggrecan measured in ng/ml

    7. Changes in serum levels of antibodies to collagen type II [Baseline, 4 weeks]

      serum levels of antibodies to collagen type II measured AU/ml

    8. Changes in serum levels of C-reactive protein [Baseline, 4 weeks]

      serum levels of C-reactive protein (CRP), g/l

    9. Changes in histamine levels [Baseline, 4 weeks]

      serum levels of histamine in ng/ml

    10. Changes in inflammation biomarkers [Baseline, 4 weeks]

      serum levels of (CRP), interleukin (IL)-6, IL- 18, adiponectin, IL-10, and interferon (IFN) γ in pg/ml

    11. Changes in neopterin levels [Baseline, 4 weeks]

      serum neopterin measured in nmol/L

    12. Changes in lipid biomarkers [Baseline, 4 weeks]

      serum total cholesterol, HDL, and LDL measured in mmol/L

    13. changes in diabetes control [Baseline, 4 weeks]

      Glycated haemoglobin (HbA1c)

    14. Changes in depression scores measured with Patient Health Questionnaire-9 (PHQ9P) [Baseline, 4 weeks]

      The PHQ-9 is a multipurpose instrument for screening, diagnosing, monitoring and measuring the severity of depression. It consists of nine questions with responses ranging from "0" (not at all) to "3" (nearly every day). The possible range is 0-27. Higher values represent worse outcome.

    15. Patient global assessment of osteoarthritis [Baseline, 4 weeks]

      The Visual Analogue Scale for the Patient global assessment of osteoarthritis varies from 0 to 10 cm. Higher values represent worse outcomes.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • osteoarthritis of the knee fulfilling American College of Rheumatology (ACR) criteria

    • diagnosis of type 2 diabetes mellitus

    Exclusion Criteria:
    • use of NSAIDs one month prior to study entry (paracetamol is allowed)

    • pregnancy and lactation

    • increased sensitivity to the study drug

    • clinically significant renal function impairment

    • use of antidepressants

    • diagnosis of bipolar disorder

    • use of symptomatic slow acting drugs of OA (SYSADOA) one month prior to study entry

    • any condition which may lead to difficulties to participation in the study from the viewpoint of Investigator

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Laboratory of Clinical Immunopharmacology Novosibirsk Russian Federation 630047

    Sponsors and Collaborators

    • Federal State Budgetary Scientific Institution, Research Institute of Fundamental and Clinical Immunology

    Investigators

    • Principal Investigator: Ivan Shirinsky, Federal State Budgetary Scientific Institution, Research Institute of Fundamental and Clinical Immunology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ivan Shirinsky, MD, PhD, Principal Investigator, Federal State Budgetary Scientific Institution, Research Institute of Fundamental and Clinical Immunology
    ClinicalTrials.gov Identifier:
    NCT03530930
    Other Study ID Numbers:
    • LCI001
    First Posted:
    May 21, 2018
    Last Update Posted:
    May 15, 2019
    Last Verified:
    May 1, 2019
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 15, 2019