CompletedN/Aketamine

Pharmacokinetics of Ketamine in Infants and Children

Sponsored by Stanford University

NCT ID
NCT00553839
Target Enrollment
21 participants
Start Date
2007-07
Est. Completion
2009-01

About This Study

Dosing of medications is based on the plasma level achieved with a given dose and how long the medicine remains in the body. This study is called pharmacokinetics-that is, what the body does to the medication. Ketamine is an intravenous medication used for anesthesia and sedation in children. However the pharmacokinetics of Ketamine has not been systematically studied. We propose to study the pharmacokinetics of ketamine in different age groups of children ranging from infants to teenagers.

Conditions Studied

The Pk of IV Ketamine in Children With Heart Disease

Interventions

  • ketamine hydrochloride

Eligibility

Age:N/A - 17 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Term infants (38 weeks gestation)and infants and children up to age 18 years.
* Patients who require procedures that necessitate at least 8 hours in the hospital and those being admitted after procedure will be eligible to participate.
* Patients who will receive ketamine as part of their standard anesthesia regimen.

Exclusion Criteria:

* Preterm neonates
* Liver Disease
* Kidney disease
* Heart failure
* Sepsis
* Patients receiving anticonvulsants or barbiturates

Study Locations (2)

Lucile Packard Children's Hospital
Palo Alto, California, United States
The Children's Hospital
Denver, Colorado, United States

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source