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临床试验/JPRN-UMIN000007719
JPRN-UMIN000007719已完成4 期

Clinical study on the analgesic efficacy of a 4-week combination of NSAIDs patch and celecoxib in patients with Knee Osteoarthritis who responded poorly to monotherapy with NSAIDs patch (A randomized, open-label, parallel-group, controlled study compared to home based exercise therapy) - Clinical study on the analgesic efficacy of NSAIDs patch and celecoxib in patients with Knee Osteoarthritis who responded poorly to monotherapy with NSAIDs patch

Sapporo Medical University School of Medicine0 个研究点目标入组 72 人开始时间: 2012年4月11日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
72

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

年龄范围
30years-old 至 90years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1)Patients diagnosed with rheumatoid arthritis, inflammatory arthritis, or gout, or those with injuries at evaluated region. (2)Patients who have received surgical or drug treatment for the evaluated knee during the study period. (3)Patients with diseases requiring continuous or intermittent steroid administration. (4)Patients requiring use of topical drugs (e.g., ointment, suppository) during the study period. (5)Patients with history of hypersensitivity to the ingredient of celecoxib, sulfonamide, or ketoprofen. (6)Patients with (history of) aspirin asthma (asthma attacks induced by NSAIDs, analgesics, etc.). (7)Patients with history of hypersensitivity to products containing tiaprofenic acid, suprofen, fenofibrate, oxybenzone, and octocrylene. (8)Patients with history of photosensitivity. (9)Patients with peptic ulcers. (10)Patients with severe hepatic disorders. (11)Patients with severe renal disorders. (12)Patients with severe cardiac dysfunctions. (13)Perioperative patients undergoing coronary artery bypass reconstruction. (14)Women at the end of pregnancy. (15)Other patients considered unsuited for the study by their doctors.

研究者

发起方
Sapporo Medical University School of Medicine

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