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Updated: Aug 11, 2026

Making MR Imaging Child's Play - Pediatric Neuroimaging Protocol, Guidelines and Procedure
Published on: July 30, 2009
Randomised double-blind clinical trial of intermediate- versus high-dose chloral hydrate for neuroimaging of children
L Martí-Bonmatí1, C L Ronchera-Oms, C Casillas
1Department of Diagnostic Radiology, Hospital Dr. Peset, Valencia, Spain.
Insights
High-dose oral chloral hydrate (100 mg/kg) significantly improved sedation success rates in children undergoing MRI compared to intermediate doses (70 mg/kg). This enhanced sedation management led to more successful MRI examinations with similar adverse reaction rates.
Area of Science:
- Pediatric imaging
- Pharmacology
- Radiology
Background:
- Chloral hydrate is a common sedative for pediatric MRI.
- Optimizing sedative doses is crucial for successful imaging and patient comfort.
Purpose of the Study:
- To compare the efficacy and safety of intermediate-dose (70 mg/kg) versus high-dose (100 mg/kg) oral chloral hydrate in pediatric MRI.
Main Methods:
- A prospective, randomized, double-blind clinical trial involving 97 children undergoing MRI.
- Children were allocated to receive either 70 mg/kg or 100 mg/kg of oral chloral hydrate.
- Sedation success, onset time, and adverse reactions were monitored.
Main Results:
- The high-dose group (100 mg/kg) showed a significantly higher success rate after the initial dose (87% vs. 64%).
- The mean time to onset of sedation was shorter in the high-dose group (21 min vs. 28 min).
- Adverse reaction rates were comparable between the two groups (20% vs. 21%).
Conclusions:
- High-dose oral chloral hydrate (100 mg/kg) is more effective for sedating children during MRI.
- This dosage improves MRI management without increasing adverse events.
- Optimized chloral hydrate dosing enhances procedural success in pediatric radiology.
Abstract:
Orally administered chloral hydrate is the most widely used sedative in children undergoing MRI. We compared intermediate- and high-dose oral chloral hydrate in 97 consecutive children undergoing MRI in a prospective, controlled, double-blind, randomised clinical trial. There were 50 girls and 47 boys, mean weight (+/- SD) 14.7 +/- 6.4 kg, and mean age 38 +/- 31. The children were randomly allocated to receive chloral hydrate syrup either 70 mg/kg (group A, n = 50) or 100 mg/kg (group B, n = 47). These two groups were not significantly different in sex, weight, age, diagnosis or ambulatory medication. The mean initial dose (+/- SEM) was 64 +/- 2 mg/kg for group A and 93 +/- 2 mg/kg for group B. Because adequate sedation was not achieved, 14 patients in group A and 6 in group B required a second dose, giving a mean total dose of 70 +/- 2 mg/kg for group A and 96 +/- 2 mg/kg for group B. The percentage of successful examinations after the initial dose (A: 64%, B: 87%; p < 0.05) and the total dose (A: 92%, B:100%; p = 0.14) was higher in group B. Significant differences were found for the time of onset of sedation (A:28 +/- 2 min, B: 21 +/- 1 min; p < 0.05), but not for the time to spontaneous awakening after the completion of the examination. The rate of adverse reactions was similar (A: 20%, B: 21%; p = 1.00). We conclude that high-dose oral chloral hydrate improves the management of children undergoing MRI.
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