EUCTR2006-001710-32-DK进行中（未招募）不适用
PeRioperative OXygen fraction – effect on surgical site Infection and pulmonary complications after abdominal surgery. (The PROXI-study) - The PROXI-study
Dept. of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet0 个研究点目标入组 1,400 人开始时间: 2006年6月21日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 1,400
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
- •Age 18 years or older.
- •Laparotomy, acute or elective. In case of gynaecological surgery only if malignancy is suspected (defined as risk of ovarian malignancy index >200 or a specimen with atypic or neoplastic cells).
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Surgery within 30 days before scheduled laparotomy (except surgery in local anaesthesia)
- •Chemotherapy within 3 months
- •Inability to give informed consent
- •Inability to keep oxygen saturation above 90% without supplemental oxygen (measured preoperatively by pulseoximetry)
研究者
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