CTRI/2012/05/002672已完成2 期
An Open Labeled, Randomized, Prospective, Multi-center, Phase II, Clinical Study to Evaluate Comparative Efficacy and Safety of Seven Different Topical Formulations in Subjects Suffering from Osteoarthritis of Knee(s) - NI
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 210
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Symptoms of osteoarthritis in one or both knee joints for a minimum of six months and maximum for five years
- •History of knee pain due to osteoarthritis requiring the use of NSAIDs, Acetaminophen, or another analgesic agent on a regular basis (greater than or equal to three days per week) for at least six months before the screening visit
- •OA confirmed by radiographs and diagnosed according to ACR diagnostic Criteria (clinical and radiological) for the osteoarthritis of the knee(s)
- •Subjects may take tab paracetamol (Less than of equal to 2g per day) for breakthrough pain
- •Subjects not having knee joint deformity
- •Subjects signing written informed consent and ready to comply with the protocol requirements
- •Subjects with pain VAS reater than 40 mm on weight bearing activities
排除标准
- •Rheumatoid arthritis, gout, pseudo gout, inflammatory arthritis, Pagets disease of bone, chronic pain syndrome, fibromyalgia, or another major joint disease
- •History of surgery, including arthroscopy, or major trauma to the study joint in the previous six months before the screening visit
- •Subjects requiring knee arthroplasty within 6 months of screening or anticipating any need for a surgical procedure on the index joint during the study
- •Signs of clinically important active inflammation of the study knee joint including redness, warmth and/or a large, bulging effusion with the loss of normal contour at the screening and/or baseline visits
- •Use of any analgesics except the study medication or paracetamol;
- •Use of systemic corticosteroids within 2 months of screening, or intra-articular viscosupplementation within the past 3 months
- •Use of any other investigational drug within 1 month prior to randomization;
- •Subjects having diabetes mellitus, tuberculosis, HIV, Ischemic Heart Disease
- •Known other major medical or surgical disease;
- •Pregnancy & Lactation.
- •Known hypersensitivity to ingredients used in study drug.
研究者
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