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临床试验/NCT05573165
NCT05573165已完成不适用

A Pilot Study of the Effects of 4 vs 3 Hours of Preoperative Fasting in Breast-feeding Infants

Uppsala University Hospital2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年1月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2
主要终点
CSA

研究概览

简要总结

In the new guideline from ESAIC breast-feeding should be encouraged until 3 hours before anesthesia. This recommendation was based mainly on gastric emptying studies in neonates with small sample sizes and single center experience.To address the lack of high quality evidence for this recommendation, the ESAIC task force for preoperative fasting plans perform a multicenter RCT omparing 4 vs 3 hours of preoperative fasting for breast milk.

The aim of the present pilot-study is to provide data for sample size calculation and feasibility for the multicenter trial.

详细描述

Since the publication of several studies indicating that many children are subjected to unnecessarily long fasting waiting for surgery, there is great interest within the pediatric anesthesia community to understand gastric emptying to be able to revise existing guidelines. The new recommendation from ESAIC is that breast-feeding should be encouraged until 3 hours before anesthesia. This recommendation was based mainly on gastric emptying studies in neonates with small sample sizes and single center experience.To address the lack of high quality evidence for this recommendation, the task force plans to perform a multicenter RCT comparing 4 vs 3 hours of preoperative fasting for breast milk.

Twenty infants scheduled for elective surgery or procedures requiring general anesthesia or sedation will be recruited for this randomized controlled pilot study.

Based on the randomization, they are then asked to breast-feed (or bottle-feed with breast-milk) the child at 4 or 3 hours before the scheduled anesthesia induction.

On arrival to the operating room, the gastric ultrasound examination will be performed for analysis of the gastric antrum CSA. After i.v. or inhalational anesthesia, an oro-gastric catheter will be inserted and any residual gastric contents are aspirated when rotating the infant from supine to semi-prone right and left positions. The volume and color of the aspirate will be recorded.

The aim of the present pilot-study is to provide data for sample size calculation and feasibility for the multicenter trial.

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
Double (Investigator, Outcomes Assessor)

盲法说明

Computerized randomization,

入排标准

年龄范围
0 Years 至 24 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Breast-feeding infanta scheduled for elective procedure requiring general anesthesia

排除标准

  • infant that does not breast-feed or is bottle-fed breast-milk
  • Moderate to severe gastrointestinal motility disorder.
  • Emergency surgery.
  • Age > 24 months or age < 37 gestational weeks
  • parents incapable of understanding the consent information due to language barrier

研究组 & 干预措施

3h Group

Experimental

the patient's parents are instructed to stop feeding 3 hours for scheduled anesthesia. (3 hours of preoperative fasting for breast milk)

干预措施: 3 hours of preoperative fasting for breast milk (Other)

4h Group

Active Comparator

the patient's parents are instructed to stop feeding 4 hours for scheduled anesthesia (4 hours of preoperative fasting for breast milk)

干预措施: 4 hours of preoperative fasting for breast milk (Other)

结局指标

主要结局

CSA

时间窗: From arrival in the operating room until induction of anesthesia

Gastric antrum CSA (The antral cross-sectional area)

次要结局

  • Aspirated volume(intraoperative)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Peter Frykholm

Assoc. Prof.

Uppsala University Hospital

研究点 (2)

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