ChiCTR1900027738Active, not recruitingNot Applicable
Individualized lung protective ventilation vs. conventional ventilation during general anesthesia in laparoscopic total hysterectomy
湖州市科学技术局1 site in 1 country60 target enrollmentStarted: December 1, 2019Last updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- 肺部并发症
Study Overview
Brief Summary
减轻术后肺部并发症
Study Design
- Study Type
- 干预性研究
- Primary Purpose
- 随机平行对照
- Masking
- 未说明
Eligibility Criteria
- Ages
- 18 to 65 (—)
- Sex
- Female
Inclusion Criteria
- •ASA 分级 I-III 级、BMI<30 kg/m2，择期腹腔镜妇科手术患者
Exclusion Criteria
- •拒绝参加本研究；严重贫血患者、合并严重心肺疾病者；合并中重度肝肾功能不全；15 天内接受过机械通气（包括 CPAP）治疗；合并需要氧疗或 CPAP 的 COPD；术后需转入 ICU；正在参加其他临床干预试验
Arms & Interventions
Group 2
保护性通气
Group 1
容量控制通气
Outcomes
Primary Outcomes
肺部并发症
Time Frame: 术后 2 天
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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