DRKS00030059尚未招募不适用
Effect of establishing a standardized, individually adapted pain therapy to reduce acute postoperative pain in ophthalmic surgery - a prospective observational study - Cologne STandardized Ophthalmic pain thErapY – Prospective observAtIoNal trial (STOP-EYE-PAIN-Trial)”
niversitätsklinikum KölnKlinik für Anästhesiologie und Operative Intensivemdizin0 个研究点目标入组 350 人开始时间: 2022年8月23日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 350
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 orbitotomy, enucleation of the eye, corneal transplantation or other eye surgery
- •Minimum age 18 years
- •Present, signed informed consent form
- •Patient consent after detailed information about the study
- •ASA classification I-III
- •50 - 120 kg body weight
排除标准
- •Intolerance to ibuprofen, metamizole, tilidine, tramadol, oxycodone, or morphine
- •Patients under 18 years of age
- •Patients who have not signed a consent form
- •Patients who could not be adequately informed due to language and comprehension problems.
- •Patients who were not cleared for surgery after the premedication visit due to their pre-existing conditions released for surgery
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