NCT05050708Unknown不适用
Risikofaktorer for Postoperativ Smerte og Kvalme Etter Dagkirurgisk Gynekologisk Laparoskopi
Oslo University Hospital1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2021年8月24日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 300
- 试验地点
- 1
- 主要终点
- postoperative pain
研究概览
简要总结
Patient due for elective, ambulatory gynaecological laparoscopy will be screened peri-operatively for known and potential risk factors of postoperative pain and nausea/vomiting.
The actual incidence and severity of pain and nausea/vomiting will be recorded during th 0-24 hr intervall after end of surgery, as well as the doses of all drugs, given for either prophylaxis or treatment
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Elective adult patients due for planned ambulatory gynaecological laparoscopy
- •Must be able to speak and write in Norwegian language
排除标准
- •Patients who, for some reason, is transferred to non-ambulatory (same day discharge) care.
- •Patients who, for some reason, have a change in surgical procedure from laparoscopy
结局指标
主要结局
postoperative pain
时间窗: 0-24 hours
Numerical Ratings Score (NRS) Scale 0-10, 10 is worst
postoperative nausea
时间窗: 0-24 hours
yes/no, Numerical Rating Score (NRS), Scale 0-10, 10 is worst
次要结局
- Post-op fatigue(0-24 hrs)
- Peri-operative nausea risk score(preop, 0-24 hours post-operatively)
- Peri-operative pain risk score(preop, 0-24 hours)
- Post-op function(0-24hr)
- Post-op anti-emetic drug consumption(0-24hr)
- Post-op analgesia consumption(0-24hr)
研究者
Johan C Ræder
professor
Oslo University Hospital
研究点 (1)
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