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Completed

NCT Number: NCT03406481

The Impact of Preoperative Fasting Period on Cardiac Index Variability After Anesthesia Induction in Pediatric Patients

The minimum period of fasting recommended by the 'American Society of Anesthesiologists' for the preoperative period is 6 hours for solid foods and 2 hours for clear liquids. Knowing the effect of preoperative fasting time on intravascular volume status may lead us to determine the amount of fluid to be administered intraoperatively. Cardiac preload static indicators are often insufficient to predict the need for fluid and are often measured by invasive methods. Knowing the adequacy of the preload is important in anesthesia practice; there is no hemodynamic benefit of fluid replacement in non-responsive patients. In this study, the investigators aimed to determine the effect of preoperative fasting period on cardiac index change after anesthesia induction in pediatric patients aged 5-12 years. The primary implication of this study is to determine the fasting period of fluid evacuation by assessing patients' intravascular volume status.

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Key information

Age range

5 year–12 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Marmara University

Istanbul, Turkey (Türkiye)

Who can participate

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

Inclusion criteria

pediatric patients, aged between 5 to 12, undergoing surgery -

Exclusion criteria

any comorbidity

-

Treatment and study plan

Primary outcomes

  1. the relationship between fasting period duration and fluid responsiveness

    Time frame: March 2018

Sponsors and collaborators

Lead sponsor

Marmara University

Other

Registry information

Important dates

Study start
2018
Primary completion
2021
Study completion
2021
First posted
Jan 23, 2018
Registry last updated
Aug 25, 2022

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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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