Gonarthrosis Clinical Trial
Official title:
Descriptive Study for the Management of Joint Pain Associated With Osteoarthritis of the Knee: Association of Extracts of Curcuma Longa, Boswellia Serrata and Porphyra Umbilicalis.
Verified date | September 2020 |
Source | Pileje |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of the study is to evaluate at 3 months the effect of a supplementation with extracts of Curcuma longa, Boswellia serrata and Porphyra umbilicalis on the acceptability of pain for patients suffering from gonarthritic pain.
Status | Completed |
Enrollment | 126 |
Est. completion date | September 5, 2019 |
Est. primary completion date | May 14, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - VAS of pain : minimum 5/10 on walking or 4/10 at rest - Patients with a negative PASS (patient considering that the symptomatic state is not acceptable) - Suffering from mono or bilateral femoro-tibial knee osteoarthrosis with painful seizures (confirmed by a radio of less than two years: stage 2 or 3 on the Kellgreen scale - clinical examination) - Having agreed to participate in the investigation after receiving information from the investigator Exclusion Criteria: - Patients with rheumatological disorders other than osteoarthritis - Patients for whom knee surgery is planned within 3 months - Patients who started treatment with chondroitin sulphate (or all treatments of osteoarthritis other than anti-inflammatories and analgesics) for less than one month - Patients with a BMI greater than 35 - Patients with chronic pain that can interfere with knee osteoarthritis pain - Patients with reduced mobility or bedridden - Patients with cognitive impairments not able to participate in the study - Patients with known allergies to any of the ingredients of Cartimotil FortĀ® - Pregnant or breastfeeding patients - Patients who do not wish to participate in the study. |
Country | Name | City | State |
---|---|---|---|
France | Pileje Network of medical practitioners in private offices | Paris |
Lead Sponsor | Collaborator |
---|---|
Pileje |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percentage of patients reaching the acceptability threshold of their state | Percentage of patients reaching the acceptability threshold of their state between D0 and D30 measured by the binary response of the PASS (yes = acceptable). | day 30 | |
Secondary | OASIS Score | Day 30 | ||
Secondary | OASIS Score | Day 60 | ||
Secondary | OASIS Score | Day 90 | ||
Secondary | Yes answer for the PASS | Day 60 | ||
Secondary | Yes answer for the PASS | Day 90 |
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