PACTR201705002263637尚未招募未知
The Effect of Premedication With Intravenous Lornoxicam on Propofol Injection Pain at Induction of General Anaesthesia in Adults; A Randomised Placebo-Controlled Trial.
Post Graduate Medical Education Programme0 个研究点目标入组 156 人开始时间: 2017年5月4日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 156
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
- 13 Year(s) 至 18 Year(s)（—）
- 性别
- All
入选标准
- •Adult patients aged 18 to 65 years
- •ASA physical status 1 and 2
排除标准
- •Systemic Arterial Hypertension.
- •History of or active phlebitis/thrombophlebitis.
- •Allergy or hypersensitivity (asthma, rhinitis, angioedema or urticaria) to lornoxicam and any of its excipients.
- •Presence of any contraindication to NSAID use and particularly:
- •Renal disease/renal impairment
- •Hypersensitivity to any other NSAIDs
- •Documented thrombocytopenia
- •Gastro-intestinal bleeding, cerebrovascular bleeding or other bleeding disorders
- •History of gastrointestinal bleeding or perforation, related to previous NSAIDs therapy
- •Active or history of recurrent peptic ulcer/haemorrhage
- •Severe hepatic impairment
- •Severe heart failure.
- •Patients already on other NSAID therapy.
- •Language barriers in eexplaining study plan and obtaining consent.
- •Difficult venous access (more than 2 attempts and/or Patients presenting for emergency surgery.
- •Patients in pain.
- •ASA physical status 3 and 4.
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