CTRI/2017/10/010142已完成4 期
Flupirtine vs Tramadol in Knee Osteoarthritis : A Randomized Controlled Trial
There was no sponsor in this trial0 个研究点目标入组 90 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 90
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Pms
入排标准
入选标准
- •1.Clinically diagnosed cases of primary early symptomatic OA affecting at least one knee joint (in case of bilateral knee involvement, the more symptomatic knee was scored as the â??signal kneeâ??).
- •2.Sex: Either sex was included
- •3. Knee joint pain present for at least one month in the preceding three months with at least one of the following: morning stiffness less than 30 min or knee crepitus
- •4.Knee pain on movement of intensity at least 35 mm on a 100 mm in VAS scale
排除标准
- •1. Secondary OA, such as due to injury, inflammatory condition, metabolic or rheumatic disease, osteonecrosis, Pagetâ??s disease, hemophilia etc.
- •2. Non-OA causes of knee pain in the signal knee (e.g. bursitis, fibromyalgia, osteonecrosis, etc)
- •3. Prior intra-articular injection of hyaluronic acid / steroid / joint lavage in the study knee any time in the past three months.
- •4. Knee injury or diagnostic arthroscopy of signal knee within 6 months preceding enrollment or knee surgery (including arthroscopic surgery requiring an incision of the internal joint components) in the study knee, at anytime.
- •5.Severe and advanced OA disease, defined as joint space width < 2 mm or deformed joint, or disease necessitating knee surgery in the current year.
- •5. Serious concomitant disease of vital organs.
- •6. Subject unlikely to provide informed consent, follow the study protocol or any other criteria, which in the opinion of the investigator, was not conducive to enrollment of a particular subject into the trial.
研究者
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