DRKS00013995招募中不适用
Effect of establishing standardized, individually adapted pain therapy versus pattern-free pain therapy to reduce acute postoperative pain after ophthalmic surgery (such as enucleation, orbitotomy, or keratoplasty) - a prospective observational study
Zentrum für Palliativmedizin der Uniklinik Koeln0 个研究点目标入组 500 人开始时间: 2018年2月8日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 500
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Patients undergoing eye surgery
- •- Present and signed informed consent
- •- Patient’s consent, after having been informed in detail on the study
- •- ASA Classification I-III
- •- 50 – 120 kg bodyweight
- •- Minimum age 18 years
排除标准
- •- Intolerance to Ibuprofene, Metamizole, Tilidine, Oxycodon or Morphine
- •- Pre-existing chronic pain
- •- Patients, who haven’t signed informed consent
- •- Patients younger than 18 years
- •- Patients, who haven’t been approved for surgery due to their pre-existing conditions after the premedication visit
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