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Effect of Premedicant Oral Paracetamol on Gastric Volume and pH

A Randomised Controlled Trial Examining the Effect of Premedicant Oral Paracetamol on Gastric Residual Volume and pH in Children, in the Context of a 1-hour Clear Fluid Fast

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04625608
Enrollment
104
Registered
2020-11-12
Start date
2020-10-06
Completion date
2021-12-31
Last updated
2021-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fasting

Keywords

general anaesthesia, children, paracetamol

Brief summary

Patients are asked to fast before general anaesthesia to reduce the risk that any gastric contents could be regurgitated and aspirated into the lungs once anaesthetised. If aspiration does occur, the volume and acidity of the fluid aspirated are thought to determine the extent of any harm caused. Recent guidelines have reduced the required fasting time for children for clear fluids from 2 hours to 1 hour before induction of anaesthesia, as it is understood that this does not adversely affect the gastric residual volume or increase its acidity. Paracetamol is commonly used to relieve pain during and after surgery. Paracetamol syrup preparations used in children are viscous and not classified as clear fluid. This study seeks to establish whether there is non-inferiority in gastric residual volume (GRV) and pH in children receiving oral paracetamol one hour before induction of anaesthesia and those who do not, when both groups have received a set volume of diluted orange cordial to drink. It is anticipated that if shown to have little or no impact on GRV and pH, oral paracetamol syrup can be given to children before surgery. This will omit the need for IV paracetamol to be given in theatre, potentially reducing cost and the risk of drug errors.

Detailed description

Patients are asked to fast before anaesthesia to reduce the risk that residual gastric contents could be regurgitated and aspirated into the lungs once anaesthetised. In animal studies, gastric contents that are less acidic (with a pH \>1.8) have been shown to be less harmful when aspirated than those that are more acidic, even at higher gastric residual volumes. Recent European and UK guidelines have reduced the length of the recommended clear fluid fast to 1 hour for children, as there is no significant difference in GRV or pH in children fasted for 1 hour compared to 2 hours. It is therefore believed to present no additional risk of harm. Some anaesthetists administer oral paracetamol syrup to children pre-operatively as an alternative to intravenous administration of paracetamol during their surgery. The oral route has been suggested to be pleasant for children, cheaper, more convenient, and reduce the risk of drug errors associated with the IV preparation. Anderson et al found no significant difference in gastric volume or pH in children with a mean age of 8.5 years given paracetamol orally 90 minutes before surgery compared to children given paracetamol rectally. Burke et al. demonstrated that giving paracetamol orally up to 8 minutes before induction of anaesthesia was not associated with an increase in the volume of stomach contents, and that the pH of stomach contents was higher than in control subjects who did not receive paracetamol. This suggests that giving oral paracetamol before induction of anaesthesia may not present any increased risk of harm from aspiration. This was in the context of a mean fluid fast of 5 hours and a mean age of 5.1 years. To our knowledge, no studies have assessed the effect of oral paracetamol syrup on gastric residual volume (GRV) and pH in the context of the newly recommended reduced clear fluid fasting time of 1 hour. Neither has this been studied in children as young as 44 weeks post-conceptual age.

Interventions

DRUGParacetamol

Standard care of 3 ml/kg water, plus 15 mg/kg oral paracetamol suspension, a minimum of 1 hour prior to the induction of general anaesthesia.

OTHERStandard care

Standard care of 3.6 ml/kg water, a minimum of 1 hour prior to the induction of general anaesthesia.

Sponsors

Barts & The London NHS Trust
CollaboratorOTHER
King's College Hospital NHS Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
44 Weeks to 8 Years
Healthy volunteers
Yes

Inclusion criteria

* Elective surgery * Requiring tracheal intubation for general anaesthesia * Parent/guardian able to speak and understand written English

Exclusion criteria

* Known or suspected gastro-intestinal disease including varices * Previous surgery which may alter gastric emptying or the anatomy of the oesophagus or stomach * Anticipated difficult airway * Concomitant administration of any other medication orally prior to anaesthesia, but excluding buccal sedative pre-medication eg midazolam * Bleeding disorders * Patients taking antacids or pro-kinetic drugs, or requiring them pre-operatively * Allergy to paracetamol * Patient weight greater than 25 kg * Parental or patient refusal

Design outcomes

Primary

MeasureTime frameDescription
Residual volume of gastric contents following induction of general anaesthesiaApproximately 5-10 minutes following the induction of general anaesthesia.Gastric volume and pH of that fluid that can be aspirated via an oro-gastric tube, passed into the patient's stomach once general anaesthesia has been induced and the airway secured.
pH of gastric contents following induction of general anaesthesiaApproximately 5-10 minutes following the induction of general anaesthesia.Gastric volume and pH of that fluid that can be aspirated via an oro-gastric tube, passed into the patient's stomach once general anaesthesia has been induced and the airway secured.

Other

MeasureTime frameDescription
Paracetamol drug errorsFor day case patients, until discharge. For inpatients, up to 24 hours post-operatively.Paracetamol related drug errors
Adverse events at induction of anaesthesiaUp to 10 minutes after the induction of anaesthesiaAdverse events occurring around the time of induction of anaesthesia including regurgitation and aspiration of gastric contents
Adverse events in Post-Anaesthesia Care UnitFrom arrival in the post-anaesthesia care unit until patient is ready for discharge to the ward, up to 24 hours.Adverse regurgitation or aspiration events occurring in the post-anaesthesia care unit, including requirements for additional analgesia, time to first analgesic request and time spent in the post-anaesthesia care unit.
Emergence deliriumUp to 10 minutes following patient arrival in PACU.Incidence of emergence delirium in post-anaesthesia care unit, measured with PAED score.
Adverse events at emergence from anaesthesiaUp to 10 minutes from removal of the patient's airwayAdverse events occurring around the time of emergence from anaesthesia including regurgitation and aspiration of gastric contents

Countries

United Kingdom

Contacts

Primary ContactEmily Saffer, MB BS
emily.saffer@nhs.net+4420 3299 9000
Backup ContactDominic PD Nielsen, MB ChB
dominic.nielsen1@nhs.net02073777000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026