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Clinical Trials/ChiCTR-OOC-14005590
ChiCTR-OOC-14005590Active, not recruitingNot Applicable

连续无创型血压监测系统(CNAP)在全身麻醉中应用的有效性研究

自费1 site in 1 country200 target enrollmentStarted: December 4, 2014Last updated:
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Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
血压
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

评价 CNAP Monitor 500 系统所测的连续无创血压（CNAP）在全身麻醉中的准确性、精确性及安全性。

Study Design

Study Type
观察性研究
Primary Purpose
单臂

Eligibility Criteria

Ages
18 to — (—)
Sex
All

Inclusion Criteria

  • •1.全身麻醉的择期手术成年患者；2.术中需行 IAP 监测的仰卧位手术；3.美国麻醉医师协会（ASA）分级Ⅰ-Ⅲ 级；4.体重指数（BMI）≤ 18-30 kg/m2；5.预计麻醉总时间大于 250 分钟；6.签署知情同意。

Exclusion Criteria

  • •1.Allen’s 试验阳性；2.存在血液透析的动静脉漏；3.雷诺综合症；4.双上肢血管病理性改变；5.研究人员认为其他原因不适合本研究者。

Arms & Interventions

连续无创血压组

连续无创血压监测

有创每搏血压组

有创每搏血压监测

Outcomes

Primary Outcomes

血压

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
自费

Study Sites (1)

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