Clinical Trials Logo

Clinical Trial Summary

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.


Clinical Trial Description

For this study, 126 patients are going to be included. They will have a supplementation of Cartimotil Fort®, from 1 to 4 capsules per day during 90 days.

on the one hand, during the two visits (inclusion and follow-up), the investigator completes the questionnaire about neuropathic pain (DN4).

on the other hand, patients complete the Osteoarthritis Symptom Inventory Scale (OASIS) 4 times : just after the inclusion visit, at day 30, at day 60 and just before the follow-up visit (day 90). He completes the Patient Global Impression of Improvement (PGII), the Minimal Clinically Important Improvement (MCII) and the Acceptable Symptomatic Statement (PASS) 6 times : just after the inclusion visit, at day 10, at day 20, at day 30, at day 60 and just before the follow-up visit (day 90). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02977936
Study type Observational
Source Pileje
Contact
Status Completed
Phase
Start date March 12, 2017
Completion date September 5, 2019

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05233930 - Total Knee Arthroplasty and Augmented Reality-based Navigation System N/A
Not yet recruiting NCT04460989 - Assessment of Patient Satisfaction After Arthroplasty: A Comparative Study by Implant Type
Recruiting NCT02411097 - Role of Femoral Nerve Block on Prevention of Postoperative Deep Venous Thromboembolism N/A
Not yet recruiting NCT05435690 - Evaluation of a New Navigation System in Computer-assisted Total Knee Arthroplasty N/A
Completed NCT06308887 - Comparison of Ultrasound-Guided Perimeniscal Steroid and 5% Dextrose Injections in Knee Osteoarthritis Phase 4
Recruiting NCT03951545 - Clinical and Radiological Impact of Tibial Cutting Int Total Knee Arthroplasty, Accelerated Navigation Versus Extramedullary Targeting N/A
Recruiting NCT06302075 - Functional Recovery After Medial Monocompartmental Knee Prosthesis: One Day Protocol Versus Fast Protocol N/A
Not yet recruiting NCT05877027 - Exercise vs. Topical Diclofenac vs. PRP N/A
Recruiting NCT04424628 - Radiotherapy 3 vs 6 Gy in Gonarthrosis and Coxarthrosis N/A
Completed NCT04577521 - The Safety and Efficacy of Single IA-HA Injection in Patients With Knee Osteoarthritis: A Prospective Study
Recruiting NCT05814471 - Validation orthèse Pour Gonarthrose N/A
Completed NCT02638831 - Ketorol Gel in Gonarthrosis and Low Back Pain Phase 4
Completed NCT01773226 - Evaluation of Intra-articular Injection of Autologous Protein Solution ("APS(TM)") for the Treatment of Osteoarthritis (OA) N/A
Recruiting NCT05062109 - Multimodal Geriatric Pre-authorization Before Scheduled Orthopedic Surgery N/A
Not yet recruiting NCT06314191 - Adipose Tissue and Symptomatic Gonarthrosis N/A
Recruiting NCT02251535 - In-vivo Comparison of Different Levels of Femoral Rollback in a Primary Total Knee Arthroplasty N/A
Active, not recruiting NCT03734315 - Routine Application of Ostenil® in Patients With Gonarthrosis
Completed NCT03389607 - The Role of SCUBE-1 in Ischemia-reperfusion Injury
Completed NCT04225182 - Evaluation of the Effectiveness of a Muscular Strengthening Protocol With an Instrumented Orthosis for Gonarthrosis Patients N/A
Recruiting NCT04313894 - WHARTON JELLY ORIGINATED MESENCHIAL STEM CELL in GONARTHROSIS Phase 2