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Clinical Trials/ChiCTR-COC-16009757
ChiCTR-COC-16009757Not yet recruitingNot Applicable

一项评估区域阻滞麻醉局麻药毒性反应与术后负性情绪关系的前瞻性队列研究

自筹1 site in 1 country200 target enrollmentStarted: November 15, 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
抑郁评分

Study Overview

Brief Summary

了解区域组织麻醉中局麻药毒性反应的发生与术后负性情绪(焦虑 / 抑郁)之间的关系。

Study Design

Study Type
病因学/相关因素研究
Primary Purpose
队列研究

Eligibility Criteria

Ages
20 to 80 (—)
Sex
All

Inclusion Criteria

  • 1.年龄 20-80 周岁(包括 20 岁、80 岁)的住院患者,男女不限,自愿参加;ASA 麻醉分级 1-3 级,
  • 2.行区域阻滞麻醉的患者;
  • 3.能够理解抑郁及焦虑的评分方法,并充足知情并签署知情同意书的患者。

Exclusion Criteria

  • 1.有局麻禁忌症(对局麻药过敏,局部炎症等)的患者;
  • 2.患有精神、神经疾病,且不能正确表达意愿者;
  • 3.药物滥用及酗酒患者;

Arms & Interventions

case series

Outcomes

Primary Outcomes

抑郁评分

Time Frame: 术后 1 天,术后 3 天,术后 3 月

焦虑评分

Time Frame: 术后 1 天,术后 3 天,术后 3 月

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
自筹

Study Sites (1)

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