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Clinical Trials/ChiCTR1900024846
ChiCTR1900024846Not yet recruitingUnknown

非药物方式对儿童术后躁动的作用:前瞻性,随机对照试验

Not provided1 site in 1 country112 target enrollmentStarted: August 10, 2019Last updated:

Trial Snapshot

Phase
Unknown
Status
Not yet recruiting
Enrollment
112
Locations
1
Primary Endpoint
苏醒期躁动发生率

Study Overview

Brief Summary

本研究的目的是探究非药物方式是否能降低儿童术后谵妄的发生率。

Study Design

Study Type
Interventional
Primary Purpose
随机平行对照
Masking
对统计者、父母及疗效评价者设盲。

Eligibility Criteria

Ages
2 to 8 (—)
Sex
All

Inclusion Criteria

  • 1 ASA 评分为Ⅰ级或Ⅱ级;

Exclusion Criteria

  • 1 耳聋或者听力障碍;
  • 2 精神发育迟缓或者精神系统疾病(精神分裂症、躁狂症、两极型异常、精神错乱等)及药物史及认知功能障碍患者;

Arms & Interventions

试验组

非药物方式(复苏期给患儿播放母亲的录音)

对照组

Outcomes

Primary Outcomes

苏醒期躁动发生率

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Not provided

Study Sites (1)

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