跳至主要内容
临床试验/NCT03399838
NCT03399838撤回4 期

The PedINDex Study: Comparing Intranasal Dexmedetomidine With Oral or Rectal Midazolam for Procedural Sedation in the Pediatric Emergency Department.

Insel Gruppe AG, University Hospital Bern0 个研究点开始时间: 2023年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
撤回
主要终点
Efficacy of procedural sedation, using the 6 point Procedural Sedation State Scale PSSS

研究概览

简要总结

This study aims to compare efficacy of Procedural Sedation with Dexmedetomidine as compared to Midazolam in the pediatric Emergency Department.

210 children aged 6 months to 6 years will be included and randomly assigned to receiving oral or rectal midazolam (standard of care) or intranasal dexmedetomidine for procedures at the emergency department where mainly a sedation and no analgesia is sought. The procedure will be videotaped and analysis is blinded to the medication.

详细描述

Pediatric sedation and analgesia is a major aspect in emergency procedures and treatments: anxiety and stress in children need to be purposefully addressed in order to perform procedures where a child needs to lie still, and to prevent anxiety in the future. An important factor to reduce stress and anxiety is the use of medication without the need of an intravenous access. To date, options for such a sedation are very limited. One of the most common medications in use is midazolam applied orally or rectally, though there are several concerns with this drug.

Pediatric developmental stage often does not allow to rationally explain procedures (e.g., wound management, emergency radiologic imaging, lumbar punctures, posing a difficult iv line), thus provoking further anxiety and non-compliance.

The medication in question (dexmedetomidine, DEX) has been proven to be a safe and reliable sedative in different settings even though its use is off-label in pediatrics. Data on its use in the pediatric emergency department (PED) are sparse, but it could be of help in a variety of situations especially in this setting.

The overall objective of this study is to determine whether intranasal (IN) DEX has better efficacy profile for PSA in the PED compared to rectal (PR)/ oral (PO) midazolam in children aged 6 months to 6 years.

Validated scores are used to describe efficacy in detail, including Procedural Sedation State Scale, Modified Yale Preoperative Anxiety Scale Short Form, University of Michigan Sedation State. Surveys to the parents and the health care professionals are used to further describe efficacy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
6 Months 至 6 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children aged between 6 months and 6 years presenting at the pediatric emergency department
  • Indication for midazolam as sedation
  • Signed informed consent

排除标准

  • Contraindication for midazolam
  • Contraindication for dexmedetomidine
  • Contraindication for moderate sedation in general

研究组 & 干预措施

Dexmedetomidine

Experimental

Application of single dose of 4mcg/kg dexmedetomidine intranasally for pediatric procedural sedation at the emergency department

干预措施: Dexmedetomidine (Drug)

Midazolam

Active Comparator

0.5mg po/pr midazolam for pediatric sedation at the emergency department

干预措施: Midazolam (Drug)

结局指标

主要结局

Efficacy of procedural sedation, using the 6 point Procedural Sedation State Scale PSSS

时间窗: Initiation of procedure, around 30 minutes after medication was given

Primary outcome is target sedation state measured with the PSSS (Pediatric Sedation State Scale) at initiation of the procedure, assessed via videotape by two independent research assistants. This scale has been developed and validated to reflect behaviours associated with adequate and inadequate sedation, in addition to adverse events associated with excessive sedation. States are predefined and related to the numbers 0 to 5. State 2 and 3 are defined as target sedation state. Primary outcome are number of patients in target sedation state.

次要结局

  • Anxiety relief, measured with a validated 18-points-observer score(Baseline, positioning for procedure, initiation of procedure, end of procedure)

研究者

申办方类型
Other
责任方
Sponsor

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