MedTrace Logo

Methadone in Pediatric Anesthesiology II

NCT01990573 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 51

Last updated 2020-01-28

Study results available
· View outcomes & findings →

Summary

Three arm randomized controlled trial to evaluate the efficacy of a single dose of intraoperative methadone in reducing post-operative pain and opioid consumption in adolescents undergoing posterior spinal fusion. Our secondary goal is to determine the pharmacokinetics of IV methadone in children (0.3 and 0.4 mg/kg).

Conditions

Interventions

DRUG

0.3mg/kg IV methadone HCl

Group I will receive 0.3mg/kg IV methadone HCl

DRUG

0.4mg/kg IV methadon HCl

Group II will receive 0.4mg/kg IV methadone HCl.

OTHER

control no methadone

The control group will not receive methadone.

Sponsors & Collaborators

  • Washington University School of Medicine

    lead OTHER

Principal Investigators

  • Anshuman Sharma, MD · Washington University School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
11 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-04-10
Primary Completion
2018-06-30
Completion
2018-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01990573 on ClinicalTrials.gov