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Clinical Trials/ChiCTR2100045788
ChiCTR2100045788Active, not recruitingEarly Phase 1

危重患儿连续性肾脏代替治疗期间液体状态评估的临床研究

重庆医科大学附属儿童医院1 site in 1 country60 target enrollmentStarted: May 1, 2021Last updated:
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Trial Snapshot

Phase
Early Phase 1
Status
Active, not recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
胸液含量
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

明确 TFC、TFCd0%、ΔTFC 是否能成为 CRRT 期间容量状态的评估指标，并指导 CRRT 期间的液体管理。

Study Design

Study Type
观察性研究
Primary Purpose
连续入组
Masking
无

Eligibility Criteria

Ages
0 to 18 (—)
Sex
All

Inclusion Criteria

  • •1.在重庆医科大学附属儿童医院重症医学科进行 CRRT 治疗；
  • •2.家属签署知情同意书。

Exclusion Criteria

  • •1.有大量胸水且未进行胸腔闭式引流；
  • •2.B 超证实心脏有严重分流；
  • •3.进行高频机械通气支持治疗；
  • •4.患儿无法保持仰卧位或胸部存在大量皮损；
  • •5.患儿对电极片过敏；
  • •6.电子心力监测法信号差。

Arms & Interventions

case series

Outcomes

Primary Outcomes

胸液含量

胸液含量变化

胸液含量与基线变化百分比

B 型钠尿肽

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
重庆医科大学附属儿童医院

Study Sites (1)

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