Skip to main content
Clinical Trials/ChiCTR1900022496
ChiCTR1900022496Not yet recruitingNot Applicable

持续泵注右美托咪定+瑞芬太尼与持续泵注右美托咪定+舒芬太尼镇静镇痛麻醉临床观察

自费1 site in 1 country100 target enrollmentStarted: April 15, 2019Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
镇痛评分

Study Overview

Brief Summary

观察两种方法镇痛镇静效果,患者血流动力学改变,并发症,用药总量有何不同。

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 60 (—)
Sex
All

Inclusion Criteria

  • 2.ASA:I~II 级
  • 3.择期在镇静镇痛麻醉下实施整形外科手术的患者。

Exclusion Criteria

  • 1.术前肝肾功能异常;
  • 2.术前存在急慢性疼痛(比如慢性腰腿痛,偏头痛等),且 48 h 内服用过镇痛药物
  • 4.患有其器质性先天性心脏病或心律失常,高血压;
  • 5.过去一个月内患过严重的肺部疾病,比如囊性纤维化,肺纤维化,肺炎;

Arms & Interventions

Group 2

持续泵注右美托咪定+瑞芬太尼

Group 1

持续泵注右美托咪定+舒芬太尼

Outcomes

Primary Outcomes

镇痛评分

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
自费

Study Sites (1)

Loading locations...

Similar Trials

持续泵注右美托咪定+瑞芬太尼与持续泵注右美托咪定+舒芬太尼镇静镇痛麻醉临床观察 | Clinical Trial