NCT02967744已完成不适用
BEVAR: Patientspecifik Behandling Ved Artrose - Et "Proof-of-concept"- Kvalitetssikringsstudie
Aalborg University1 个研究点 分布在 1 个国家目标入组 162 人开始时间: 2016年1月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 162
- 试验地点
- 1
- 主要终点
- Pain intensity measured on a 10cm visual analog scale
研究概览
简要总结
The study investigates associations between pre treatment pain intensity and central pain mechanisms on the effect of 8-week treatment of NSAIDs in patients with knee osteoarthritis.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosed Knee Ostoarthritis
排除标准
- •Current ulcer diagnosed by endoscope
- •Asthma or other allergic reaction to NSIADs
- •Kidney disease
- •Myocardial infarction within the last six months
- •Severe hyper tension (systolic ≥180mmHg, diastolic ≥110mmHg)
- •Severe thrombocytopenia (thrombocyst count <50x10^9/l)
- •Insufficience lever or kidney function
研究组 & 干预措施
NSAID treatment
Experimental
8 weeks of NSAID treatment
干预措施: NSAID (Drug)
结局指标
主要结局
Pain intensity measured on a 10cm visual analog scale
时间窗: 8 weeks after treatment
Patients will be asked to rate the pain intensity 8 weeks after treatment on a 10cm visual analog scale (0 indicating no pain, 10 indicating worst imaginable pain
次要结局
未报告次要终点
研究者
Kristian Kjær Petersen
assistant professor
Aalborg University
研究点 (1)
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