Joint Pain, Pain
Conditions
Keywords
Pain, Arthritis, Knee
Brief summary
This clinical trial aims to evaluate the antalgic effect of Puressentiel Joints and Muscles - Gel with 14 essential oils for 12 weeks on knee joint pain in 45 patients suffering from chronic pain related to arthritis of the knee. The evaluation of the puressentiel antalgic effect Joints and Muscles - Gel with 14 essential oils will be done by an algo-functional score of WOMAC based on items of pain, joint stiffness and locomotor function (main criterion), a visual analog scale EVA (graduated from 1 to 10) of the pain by self-assessment of the patient during the consultation and the number of daily analgesics and anti-inflammatory drugs (secondary criteria).
Detailed description
This clinical trial aims to evaluate the antalgic effect of Puressentiel Joints and Muscles - Gel with 14 essential oils for 12 weeks on knee joint pain in 45 patients suffering from chronic pain related to arthritis of the knee. The patients included in the study will be consultants from the Department of Physical Medicine, Rehabilitation and Sports Trauma at Foch Hospital in Suresnes and will have to present chronic pain related to arthritis of the knee either with or without antalgic and anti-inflammatory treatment. The evaluation of the puressentiel antalgic effect Joints and Muscles - Gel with 14 essential oils will be evaluated by an algo-functional score of WOMAC based on items of pain, joint stiffness and locomotor function (main criterion), a visual analog scale EVA (graduated from 1 to 10) of the pain by self-assessment of the patient during each visit and the number of daily antalgic and anti-inflammatory drugs (secondary criteria).
Interventions
DEVICEJoint and muscle gel Puressentiel
To evaluate the antalgic effect in patients with chronic pain related to osteoarthritis of the knee when applied to the skin of Puressentiel Joints and Muscles - Gel with 14 essential oils.
Sponsors
Marco Pacchioni
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
open single arm study
Eligibility
Sex/Gender
ALL
Age
45 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
* Subject smust be able to understand the terms of the written informed consent and must agree to date and sign it before any study procedure is carried out, * Patient having signed the informed consent * Aged 45 to 90 * With chronic osteoarthritis of the knee * Patient with or without analgesic and anti-inflammatory treatment
Exclusion criteria
* Patient at the stage of surgical osteoarthritis (grade 4 plus limitation of amplitude) * Patient with a limited walking perimeter (\<100m) for any reason whatsoever * Patient allergic to one of the components of the study product * Patient not benefiting from social security * Patient cannot be followed for the duration of the study * Participation in another clinical trial within 30 days before V0 * Subjects who cannot understand or perform study procedures. * Pregnant or breastfeeding women * People with a history of convulsive or epileptic disorders * People allergic to salicylates.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Womac score is the primary outcome | 30 days | Scoring pain and locomotion with a maximum score (worse of 96). A change of 16 points is considered as a significant clinical improvement |
| Pain visual analog analog scale is the secondary outcome | 30 days | Scoring pain from 1 to 100 (worse) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pain visual analog scale | Evaluation at inclusion and after 30 days | Pain visual analog scale scored from 0 to 100(worse). A change of 10 points is considered as clinically significant |
Countries
France
Contacts
Backup ContactElisabeth Simon
Primary ContactElisabeth Simon, MD
Outcome results
None listed