Pharmacokinetics of Multiple Dose Methadone in Children Treated for Opiate Withdrawal (MTH01)

Kevin Watt

Status: Completed

Conditions: Opiate Withdrawal Syndrome

Treatments: Drug: Methadone

Study type: Observational

Funder types: Other; NIH

Identifiers

NCT01945736

HHSN27500021 (Other Identifier)

Pro00044082

Details and patient eligibility

About

The purpose of this study is to learn more about how the study drug, methadone, prescribed by an infant's or child's physician as part of standard medical care, is processed in children and young adults. While this drug is used extensively in infants and children, it has not been extensively studied in this population.

Physicians do not have very much information on how long it takes for methadone to be removed from the blood circulation and passed out of the body. Physicians need more information to guide how much and how often we should give methadone to children/young adults to ensure they get the maximum effect with the minimum amount of drug. During this research study, the study team will collect information about how this drug is processed in infants and children.

Full description

A total of approximately 24 to 36 infants and children will participate in this study. This study will be done at five medical centers in the United States.

Treatment will be prescribed by the infant or child's doctor and not by the study team.

Participants will be divided into 3 groups based on age, ages 3 months to 2 years, ages 2 to 6 years, and ages 6 to 18 years. There will be approximately 8 to 12 participants enrolled in each group. Additionally, at least 6 overweight or obese participants between ages 2-18 years will be included in this study.

Information collected from each subject's routine medical care will include:

• Participant gender, date of birth, race and ethnicity
• Pertinent medical history
• Laboratory results (blood count and chemistries) from routine testing ordered by the infant or child's regular doctor
• Medications of interest the child was given within the 72 hours prior to first dose of methadone administered after consent
• Time and dose of methadone administered to the child up to 14 days prior to enrollment

Study specific information collected will include:

• Blood sample collection to measure level of methadone
• Baseline WAT-1 score (sedation withdrawal assessment of the infant or child used to assess symptoms the child/infant may experience when opioid drugs are discontinued).

The duration of the study will be up to 10 days, comprised of a maximum 5 day treatment period a 5 day observation period.

Enrollment: 26 patients

Sex: All

Ages: 91 days to 18 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• >90 days - < 18 years of age at the time of first dose of study drug
• Receiving enteral methadone as standard of care
• Signed informed consent/HIPAA documents by the parent/legal guardian and assent (if applicable)

Exclusion criteria

• Previous participation in the study
• Subject is receiving ECLS (Extracorporeal Life Support)
• < 36 weeks gestational age at birth for children <1 year of age at time of enrollment
• Any other condition or chronic illness that in the opinion of the Principal
• Investigator makes participation unadvised or unsafe

Trial design

26 participants in 3 patient groups

Cohort 1

Description:

\> or = 90 days to \< 2 years on enteral methadone. Dose schedule is per routine medical care.

Treatment:

Drug: Methadone

Cohort 2

Description:

2 years to \< 6 years on enteral methadone. Dose schedule is per routine medical care. Will include overweight children with BMI for age of 85 - 95 percentile, or obese children BMI for age \> or = to 95 percentile.

Treatment:

Drug: Methadone

Cohort 3

Description:

6 years to \< 18 years on enteral methadone. Dose schedule is per routine medical care. Will include overweight children with BMI for age of 85 - 95 percentile, or obese children BMI for age \> or = to 95 percentile.

Treatment:

Drug: Methadone