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Evaluation of the Efficacy and Safety of Nise 100 mg in the Management of Osteoarthrosis (Gonarthrosis)

Evaluation of Clinical Efficacy and Safety of the Drug Nise (Nimesulide) in Complex Treatment of Patients With Osteoarthritis of the Knee and Hip Joints

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02922712
Acronym
NISE-2013
Enrollment
202
Registered
2016-10-04
Start date
2011-03-31
Completion date
2013-08-31
Last updated
2016-10-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

Brief summary

Study is conducted to evaluate safety and efficacy in patients with osteoarthritis

Detailed description

Osteoarthritis is the most common disorders of the joints, which gives a page more than 10% of the world population aged over 45 years (Woolf A. D., Pfleger B., Bergman S., 2009). The main clinical manifestations of the disease are pain in the joints and a violation of their functions. Therefore, one of the first tasks in the therapeutic program, these patients will decrease and possible pain relief. Nesteroi dnye anti-inflammatory drugs (NSAIDs) are the main group of medicines drugs used in medical practice in lech th Research Institute of pain in patients with lesions of the musculoskeletal system. The basis of the therapeutic effect of the second of these drugs is the suppression of the activity of Fe p IU NTA cyclooxygenase (COX). Prichё m, the suppression of the activity of COX-2 isoenzyme involved in the synthesis of prostaglandins, induce the development of pain and PLAYBACK tion and provides anti-inflammatory effects of NSAIDs. B Blocking out of the enzyme COX-1, which controls the synthesis of prostaglandins, have cited a protective properties, leading to side effects of NSAIDs These so called nye formed the basis for the creation of new NSAIDs that can selectively inhibit COX-2 and m and mally affect COX. - 1. Nimesulide is a selective inhibitor of cyclooxygenase -2 vnym with Sat and anced analgesic and anti-inflammatory effect, but also has antibradikinin, antihistamine and antioxidant activity of Stu(Nasonov EL, 1999, 2001).

Interventions

DRUGNISE

Nise 200mg Max per day in 2 divided doses

Sponsors

Dr. Reddy's Laboratories Limited
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* patients 40 years old and older with verified diagnosis of OA of the knee joints according to the criteria of American College of Rheumatology (АСR); * radiologic abnormalities complying with I-III grades of Kellgren; * pain syndrome not less than 40 points according to 100-point visual analogue scale (VAS).

Exclusion criteria

* A history of the patient within the last 5 years malignancy of any organ or system regardless of whether the treatment and is carried on this occasion elk. * The presence of acute ulcer disease of the gastrointestinal tract that is, over several recent years. * Any data on the bleeding from the upper gastrointestinal tract. * Severe disease: uncontrolled hypertension, expression n naya cardiovascular failure, a pathology of the hematopoietic system, and mellitus type I, and others. * The presence of other rheumatic diseases with the exception of teoartroza. * Liver disease (cirrhosis, chronic hepatitis). * Abnormal liver function (ALT, AST, bilirubin more than 1.5 times the upper limit of normal). * Impaired renal function (blood creatinine more than 1.5 times higher than it's ver limit of normal). * Anemia (g emoglobin more than 10 g / l less than the lower limit of normal). * Treatment with corticosteroids (systemic reception), warfarin and other coumarin governmental produ d. * Hypersensitivity to the analgesic and antipyretic Wed d stvam, NSAIDs, sulfonamides. * Pregnancy and lactation. * Alcohol and drug abuse history.

Design outcomes

Primary

MeasureTime frame
Mean Pain Intensity on VASFrom baseline to 3 week

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026