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Completed

NCT Number: NCT05573165

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

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.

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Key information

Age range

0 year–24 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Uppsala University Hospital

Uppsala, 75185, Sweden

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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

Treatment and study plan

3 hours of preoperative fasting for breast milk

Other

3 hours of preoperative fasting for breast milk

4 hours of preoperative fasting for breast milk

Other

4 hours of preoperative fasting for breast milk

Primary outcomes

  1. CSA

    Time frame: From arrival in the operating room until induction of anesthesia

    Gastric antrum CSA (The antral cross-sectional area)

Secondary outcomes

  1. Aspirated volume

    Time frame: intraoperative

    Aspirated volume

Sponsors and collaborators

Lead sponsor

Uppsala University Hospital

Other

Registry information

Acronym: BMRCT

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Oct 10, 2022
Registry last updated
Mar 22, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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