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Clinical Trials/ChiCTR2200063099
ChiCTR2200063099Not yet recruitingPhase 1

规模化儿童镇静技术

自筹1 site in 1 countryStarted: September 1, 2022Last updated:

Trial Snapshot

Phase
Phase 1
Status
Not yet recruiting
Sponsor
Locations
1
Primary Endpoint
镇静成功率

Study Overview

Brief Summary

规模化儿童镇静方法在无痛性检查中的应用。

Study Design

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

Eligibility Criteria

Ages
0 to 6 (—)
Sex
All

Inclusion Criteria

  • ASA 分级 I-II 级;
  • 在镇静下接受头颅 MRI 检查。

Exclusion Criteria

  • 鼻黏膜、口腔粘膜损伤;

Arms & Interventions

2 组

1 组

Outcomes

Primary Outcomes

镇静成功率

Time Frame: 完成检查

镇静诱导时间

Time Frame: 诱导入睡时间

镇静时间

Time Frame: 呼唤清醒

不良反应

Time Frame: 镇静后 1 日

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
自筹

Study Sites (1)

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