RecruitingPhase 4ACTRN12619000612112

One-Needle Approach to Paediatric Procedural Sedation using Ketamine: A Randomised Control Trial.


Sponsor

Gold Coast Hospital and Health Service

Enrollment

537 participants

Start Date

Jul 31, 2019

Study Type

Interventional

Conditions

Summary

Procedural sedation in children is a commonly performed task in mixed emergency departments around Australia. Ketamine has gained significant acceptance as the drug of choice to conduct this sedation. The preferred route of ketamine administration is an ongoing debate. Historically intravenous ketamine sedation has been favoured, however the evidence is not strong and mostly based on anecdotes. Further, the initial intravenous cannulation required has the negative consequence of inducing significant pain and distress. Aim To demonstrate in a randomised control trial that intramuscular ketamine, given in one needle, can achieve successful procedural sedation in children. Research Design This is an open label multicentre randomised control trial investigating whether paediatric procedural sedation can be achieved with just one needle. Study sites include Gold Coast University Hospital and Logan Hospital - 537 participants will be enrolled. Patients 1-12 yrs of age presenting to emergency department and requiring procedural sedation with ketamine (as determined by the senior treating clinician) will be eligible for inclusion into the study. Exclusion criteria will include the lack of informed consent and intravenous cannulation being required for another aspect of their management. The study has two intervention arms, one arm will receive 3mg/kg and the other arm will receive 4mg/mg via intramuscular injection. Participants will be randomised in a 1:1:1 ratio between the two intervention arms and control. Intramuscular injections will be administered by the treating doctor or nurse. Where adequate sedation to undertake the required procedure is not achieved with the initial intramuscular dose, additional intramuscular or intravenous doses of ketamine will be administered at treating clinician discretion.. Patients in the control group will be intravenously cannulated and ketamine given initially at 1mg/kg and then dose titrated to effect at the treating clinician’s discretion. The primary outcome will be success of paediatric procedural sedation with only one needle. Secondary outcomes include length of stay in the emergency department, length of sedation and adverse effects in the intramuscular versus intravenous groups. Significance This multicentre randomised trial will allow definitive assessment of the efficacy of a one needle approach giving intramuscular ketamine to achieve paediatric procedural sedation in children, with the goal of minimising unnecessary distress.


Eligibility

Sex: Both males and femalesMin Age: 1 YearsMax Age: 12 Yearss

Plain Language Summary

Simplified for easier understanding

This study is comparing two approaches to giving the sedative drug ketamine to children who need a procedure done in the emergency department — such as setting a broken bone or stitching a wound — that would otherwise be too painful or frightening without sedation. The traditional approach uses an intravenous (IV) drip, which itself requires inserting a needle into a vein, causing additional pain and distress. The study tests whether giving ketamine as a single intramuscular (muscle) injection can sedate children just as effectively while sparing them the extra needle. Children aged 1–12 who present to Gold Coast University Hospital or Logan Hospital emergency department needing sedation will be randomly assigned to receive intramuscular ketamine at one of two doses, or intravenous ketamine as the control. The main outcome is whether adequate sedation is achieved with just one needle. Your child may be eligible if they are between 1 and 12 years old, weigh under 50 kg, need procedural sedation with ketamine, and do not have a known ketamine allergy. Children who need an IV line for other reasons (such as antibiotics or fluids) cannot participate, as they would need a needle anyway. This multicentre trial aims to find a kinder way to help children through painful emergency procedures.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

The study has two intervention arms, one arm will receive 3mg/kg via intramuscular injection and the other arm will receive 4mg/mg via intramuscular injection. Participants will be randomised in a 1:1

The study has two intervention arms, one arm will receive 3mg/kg via intramuscular injection and the other arm will receive 4mg/mg via intramuscular injection. Participants will be randomised in a 1:1:1 ratio between the two intervention arms and control. Intramuscular injections will be administered by the treating doctor or nurse. Where adequate sedation to undertake the required procedure is not achieved with the initial intramuscular dose, additional intramuscular or intravenous doses of ketamine will be administered at treating clinician discretion.


Locations(2)

Gold Coast University Hospital - Southport

QLD, Australia

Logan Hospital - Meadowbrook

QLD, Australia

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ACTRN12619000612112


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