Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This study is conducted to study the efficacy and safety of Niselat in patients with osteoarthritis.
Osteoarthritis is the most common rheumatic disease. Knee OA (KOA), gonarthrosis (GA), is characterized by high prevalence, progressive course with early disability of the subject, persistent pain syndrome for the treatment of which non-steroidal anti inflammatory drugs (NSAIDs) are actively used in clinical practice. It was revealed that NSAIDs may cause gastrointestinal adverse effects (AEs), from mild dyspepsia to bleeding and perforation as well as cardiovascular effects. Gastroprotection with misoprosol, Н2-receptor antagonists and proton pump inhibitors (PPI) is not always effective. NSAIDs with the lowest gastrointestinal toxicity with efficacy adequate to suppress joint pain is justified and reasonable.
Amtolmetin guacil (AMG) is a new NSAID which proved to be the least gastrointestinally toxic in experimental studies in vivo, in vitro and in comparative clinical studies. AMG does not have selectivity towards COX-2 or NO. AMG exerts gastroprotective effect due to stimulation of capsaicin receptors (vanilloid receptors) in gastrointestinal wall. To assess tolerability of amtolmetin guacil, it is first necessary to obtain data on potential reduction of dyspeptic symptoms including in subjects with these signs of NSAIDs intolerability.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NISELAT | Amtolmetin guacil should be taken in fasting conditions. The recommended dose is 600 mg b.i.d. Maximum daily dose - 1800 mg |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| NISELAT | Drug | NISELAT 600MG BD |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Reduction in WOMAC score from baseline | Reduced WOMAC (according to pain, rigidity and function scales) by > 20 % vs. baseline. | Baseline to 4 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in VAS | Baseline to 45 weeks | |
| SODA Questionnaire | Baseline to 4weeks | |
| No of adverse events |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Subjects with knee osteoarthrosis (KOA)
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Denisov L Nikolaevich, MD | Moscow, Federal State Budget Scientific Institution "Scientific Research Institute of Rheumatology named VA Nasonova" | Principal Investigator |
Not provided
Under review
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D020370 | Osteoarthritis, Knee |
| ID | Term |
|---|---|
| D010003 | Osteoarthritis |
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
Not provided
Not provided
Total number of adverse events
| Baseline to 4 week |
| D012216 |
| Rheumatic Diseases |