EUCTR2015-002239-16-DK进行中（未招募）1 期
PANSAID – PAracetamol and NSAID in combination: A randomised, blinded, parallel 4-group clinical trial - PANSAID
æstved Hospital0 个研究点目标入组 556 人开始时间: 2015年6月8日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 556
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Scheduled for unilateral, primary THA
- •ASA 1-3.
- •BMI > 18 and < 40
- •Women in the fertile age must have negative urine HCG pregnancy test
- •Patients who gave their written informed consent to participating in the trial after having fully understood the contents of the protocol and restrictions.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 156
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 400
排除标准
- •Patients who cannot cooperate with the trial.
- •Concomitant participation in another trial
- •Patients who cannot understand or speak Danish.
- •Daily use of strong opioids (tramadol and codein are accepted)
- •Patients with allergy to the medicines used in the trial.
- •Contraindications against NSAID or paracetamol, for example previous ulcer, heart failure, liver failure, or renal failure (eGRF < 60 ml/kg/1,73m2), known thrombocytopenia (<100 mia/L)
- •Patients suffering from alcohol and/or drug abuse – based on the investigator's judgement.
研究者
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