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Clinical Trials/ChiCTR1900024789
ChiCTR1900024789Active, not recruitingEarly Phase 1

脑电监测及手术体积描记指数用于全麻患者镇痛监测的研究

基于高密度脑电分析精确预测和诊断老年患者术后谵妄和认知功能1 site in 1 country80 target enrollmentStarted: April 1, 2019Last updated:

Trial Snapshot

Phase
Early Phase 1
Status
Active, not recruiting
Sponsor
Enrollment
80
Locations
1
Primary Endpoint
疼痛指数

Study Overview

Brief Summary

为探讨 SPI 及脑电监测对于全麻患者镇痛效果监测的可靠性和有效性,及与术后急性期疼痛的相关性。

Study Design

Study Type
观察性研究
Primary Purpose
连续入组
Masking
N/a

Eligibility Criteria

Ages
40 to 80 (—)
Sex
All

Inclusion Criteria

  • 年龄 40-80 岁,男女不限、右利手;拟在全身麻醉下行择期腹腔镜手术的泌尿外科住院病人;ASA 分级 I-II 级

Exclusion Criteria

  • 术前慢性疼痛病史;精神神经疾病史;严重心血管疾病史;药物依赖史;酗酒史;2 周内任何药物服药史;近 3 月参加其他临床试验者;妊娠哺乳期患者。

Arms & Interventions

Case series

EEG 和 SPI

Outcomes

Primary Outcomes

疼痛指数

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
基于高密度脑电分析精确预测和诊断老年患者术后谵妄和认知功能

Study Sites (1)

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