Multicenter Perioperative Opioid Pharmacogenetic Study

NCT01495611 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2017-01-31

No results posted yet for this study

Summary

The purpose of this research study is to identify factors and genes (the DNA material that determines the makeup of the human body) that may be associated with how children respond to pain medication. Specifically, the investigators want to study factors that may be associated with pain sensitivity, morphine requirement after surgery and side-effects from morphine and other pain medications. The investigators expect that the information obtained in this research study will help us to develop more effective, safe, and tailored treatment options in the future.

Conditions

Sponsors & Collaborators

  • Baylor College of Medicine

    collaborator OTHER
  • Ochsner Health System

    collaborator OTHER
  • Children's Hospital Colorado

    collaborator OTHER
  • Children's Hospital Los Angeles

    collaborator OTHER
  • C.S. Mott Children's Hospital

    collaborator OTHER
  • St. Christopher's Hospital for Children

    collaborator OTHER
  • St. Louis Children's Hospital

    collaborator OTHER
  • Boston Children's Hospital

    collaborator OTHER
  • Seattle Children's Hospital

    collaborator OTHER
  • Ann & Robert H Lurie Children's Hospital of Chicago

    collaborator OTHER
  • University of Wisconsin, Madison

    collaborator OTHER
  • University of Miami

    collaborator OTHER
  • Johns Hopkins University

    collaborator OTHER
  • Stanford University

    collaborator OTHER
  • Phoenix Children's Hospital

    collaborator OTHER
  • University of Michigan

    collaborator OTHER
  • University of Utah

    collaborator OTHER
  • Shanghai Children's Hospital

    collaborator OTHER
  • Children's Hospital Medical Center, Cincinnati

    lead OTHER

Principal Investigators

  • Senthilkumar Sadhasivam · Children's Hospital Medical Center, Cincinnati

Eligibility

Min Age
6 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2016-01-31
Completion
2017-04-30

Countries

  • United States

Study Locations

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Entities

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 NCT01495611 on ClinicalTrials.gov