Pharmacokinetics of Intravenous Metamizole in Children Less Than 6 Years Old

Phase 2

Completed

• Conditions: Children; Pain; Surgery
• Interventions: Drug: Metamizole

• Registration Number: NCT02660177
• Lead Sponsor: University Children's Hospital Basel

Brief Summary

This study aims to assess the PK parameters of metamizole following a single IV administration of metamizole in children less than 6 years of age.

Detailed Description

This is an open-label pharmacokinetics (PK) study. It aims to assess the PK parameters of metamizole and its metabolites following a single IV administration of metamizole (10mg/kg) in children less than 6 years of age.

Thirty-nine children, 3-72 months of age, undergoing elective surgery at the University of Basel Children's Hospital, will receive, on the day of surgical procedure, a single dose of metamizole 10 mg/kg. After this dose, blood and saliva samples will be obtained at predetermined post-dose time points to measure concentrations of metamizole and its metabolites. The maximal duration of subject participation will be 24 hours. Plasma PK parameters (AUC, Cmax, Tmax, t1/2) of each analyte will be derived using noncompartmental methods. A population PK approach will be applied to characterize inter-subject variability and quantify the potential influence of age, sex and body weight on the PK parameters.

There are no published pharmacokinetic studies of metamizole in pediatrics. Furthermore, although Swissmedic provides no dose information for IV administration in infants with a body weight of less than 9 kg, IV is the most frequently used route of administration for direct postoperative analgesia in pediatrics, including infants with body weights of less than 9 kg. Due to the absence of data and the lack of any dosing recommendation for infants with a body weight less than 9 kg, the IV administration of metamizole in infants is "off-label" and inconsistent across hospitals and prescribing paediatricians.

Study Timeline

• Study First Submitted: 2016-01-14
• Study First Submitted QC: 2016-01-18
• Study First Posted: 2016-01-21
• Study Start: 2016-04
• Primary Completion: 2017-12
• Study Completion: 2017-12
• Status Verified: 2018-05
• Last Update Submitted: 2018-05-28
• Last Update Posted: 2018-05-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 33

Inclusion Criteria

• Infants and children 3-72 months of age at time of inclusion
• Body weight more than 5 kg at time of inclusion
• Children undergoing elective surgery at University of Basel Children's Hospital (UKBB) with planned administration of intravenous analgesia
• Patients who require surgical procedures that necessitate at least 24 hours in the hospital
• Parent/Legal guardian has been informed about the study and has signed Informed Consent Form

Exclusion Criteria

• Infants and children who were born prematurely (before 37 weeks gestation), regardless of corrected gestational age
• Known kidney or liver disease
• Known neutropenia, anemia or other hematological disorders
• Known diagnosis of asthma
• Ongoing immunosuppression, except corticosteroid treatment, or primary immunodeficiency
• Treatment with strong inhibitors or inducers of CYP2C19 within 3 months prior to study
• Treatment with drugs known to induce agranulocytosis within 3 months prior to study
• Documented previous adverse reaction to metamizole
• Treatment with metamizole within 30 days prior to screening
• Any concomitant condition, which in the opinion of the investigator would preclude a subject's participation in the study
• Family members of investigators

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
metamizole	Metamizole	single IV metamizole (10mg/kg) administration

Primary Outcome Measures

Name	Time	Method
Area under the plasma concentration-time curves (AUC0-inf, AUC0-24, AUC0-last) for metamizole and its metabolites in plasma and saliva	0- 24 hours	Time points of evaluation of these PK parameters: sampling at 1, 2, 4, 6, 10 and 24 hours after single IV metamizole dose.

Secondary Outcome Measures

Name	Time	Method
Incidence of adverse events (AEs)	0- 24 hours
Maximum plasma concentration (Cmax) for metamizole and its metabolites in plasma and saliva	0- 24 hours	Time points of evaluation of these PK parameters: sampling at 1, 2, 4, 6, 10
Time to reach Cmax (tmax) for metamizole and its metabolites in plasma and saliva	0- 24 hours	Time points of evaluation of these PK parameters: sampling at 1, 2, 4, 6, 10
Terminal elimination rate constant with respective half-life time (t½) for metamizole and its metabolites in plasma and saliva	0- 24 hours	Time points of evaluation of these PK parameters: sampling at 1, 2, 4, 6, 10
Correlation between metamizole and its metabolites in saliva and plasma	0- 24 hours

Trial Locations

Locations (1)

UKBB; 🇨🇭 Basel, Switzerland