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Clinical Trials/ChiCTR-IOR-17011776
ChiCTR-IOR-17011776Not yet recruitingNot Applicable

尼莫地平对全麻老年患者术后谵妄的影响

河北省政府资助临床优秀人才培养和基础课题研究项目(361005)1 site in 1 country60 target enrollmentStarted: August 1, 2017Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
认知功能

Study Overview

Brief Summary

本研究拟评价尼莫地平对全麻老年患者术后谵妄的影响。

Study Design

Study Type
干预性研究
Primary Purpose
随机平行对照

Eligibility Criteria

Sex
All

Inclusion Criteria

  • (1)在全身麻醉下接受腰后路减压植骨融合内固定术的老年腰椎间盘突出症患者,(2)无脑损伤,神经疾病及酗酒史,(3)术前无认知功能障碍,(4)无视觉和听力损伤,无明显的心肺肝肾功能异常

Exclusion Criteria

  • (1)手术时间超过 3 小时,(2)术中出血量超过 800ml,(3)手术因各种原因被取消

Arms & Interventions

对照组

标准治疗

尼莫地平组

尼莫地平预处理

Outcomes

Primary Outcomes

认知功能

Time Frame: 术后 1-7 天

S100β

Time Frame: 尼莫地平给药前即刻、气管插管后即刻、切皮后 1 小时及术毕

胶质细胞原纤维酸性蛋白

Time Frame: 尼莫地平给药前即刻、气管插管后即刻、切皮后 1 小时及术毕

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
河北省政府资助临床优秀人才培养和基础课题研究项目(361005)

Study Sites (1)

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