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  3. Study of the Effects of Pantoprazole on Levels of Prescribed Psychiatric Medications (PK-PPI)
Research Study

A Pilot Study to Determine if Pantoprazole Modifies Steady-State Plasma Concentrations of Orally Administered Psychotropic Medications

Principal Investigator
Ric Procyshyn

Overview

Body Locations and Systems
Brain
Disorders and Conditions
Mental Health
ClinicalTrials.gov#
NCT02213887
Status
Closed for Recruitment
Start/End Dates
Sep 1, 2014
Locations
St. Paul's Hospital
UBC Hospital
Name/Title
Heidi Boyda, Post Doctoral Fellow
Phone
604-822-7500
Email Address
hnboyda@gmail.com
Purpose of Study

The purpose of this 9-day study is to determine if:

  • Pantoprazole modifies the steady-state plasma concentrations of orally administered psychotropic medications including valproic acid, lithium, and second-generation antipsychotics (i.e., aripiprazole, asenapine, clozapine, lurasidone, olanzapine, paliperidone, quetiapine, risperidone, ziprasidone)
  • Serum gastrin levels change within a week of starting or stopping pantoprazole
Eligibility

Visit ClinicalTrials.gov for more information.

Disclaimer

Study Coordinators and Research Nurses cannot give medical advice over the phone. Telephone numbers and email addresses are provided for obtaining additional information on specific clinical research trials only. If you have specific questions which require clinical expertise, please call your primary care physician.

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