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Determining Metabolic Effects of Valproate and Antipsychotic Therapy

Primary Purpose

Schizophrenia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Valproate
Placebo
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Diabetes, Metabolic

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Meets DSM-IV criteria for schizophrenia, any type, treated with the same antipsychotic for at least 6 months No antipsychotic medication dose changes for 1 month, and no other medication changes for 1 month prior to study entry Exclusion Criteria: Meets DSM-IV criteria for substance abuse within 3 months of study entry Involuntary legal status (as per Missouri law) Any serious medical disorder that may confound the assessment of relevant biologic measures or diagnosis, including: significant organ system dysfunction, metabolic diseases, type 1 or 2 diabetes mellitus, pregnancy, endocrine disease, coagulopathy, anemia, or acute infection Currently taking more than one antipsychotic medication Currently taking prescription medications (except certain psychotropic medications as discussed below), including oral contraceptive pills, any glucose lowering agent, lipid lowering agent, exogenous testosterone, recombinant human growth hormone, or any other endocrine agent that might confound substrate metabolism

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Experimental

Arm Description

50% of participants will receive placebo

50% of participants will receive Depakote ER

Outcomes

Primary Outcome Measures

Change From Baseline in Total Body Fat Composition Using Dual Energy X-ray Absorptiometry at 12 Weeks
Change in body composition (total body fat) was assessed using dual energy x-ray absorptiometry
Effects of Medication on Insulin Secretion at Skeletal Muscle (Glucose Disposal)

Secondary Outcome Measures

Full Information

First Posted
September 9, 2005
Last Updated
January 28, 2020
Sponsor
Washington University School of Medicine
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00167934
Brief Title
Determining Metabolic Effects of Valproate and Antipsychotic Therapy
Official Title
Metabolic Effects of Valproate and Antipsychotic Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
December 2004 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will determine the metabolic processes responsible for high levels of blood glucose, metabolism disorders, and weight gain in people with schizophrenia who have been treated with antipsychotic medications in combination with valproate.
Detailed Description
This project aims to study the whole-body metabolic processes responsible for hyperglycemia, dyslipidemia and increased adiposity in schizophrenia patients treated with antipsychotic medications in combination with valproate. The project hypothesizes that combined treatment with valproate and antipsychotic medications will decrease insulin sensitivity at the level of skeletal muscle, liver and adipose tissue, in comparison to antipsychotic monotherapy. The decrease in insulin sensitivity is hypothesized to be associated with defects in glucose and lipid metabolism and increased adiposity Treatment effects of antipsychotic/valproate combination therapy on different components of insulin secretion and action, and treatment effects on abdominal versus peripheral adiposity, are unknown despite the availability of gold-standard methods and the prognostic significance of these issues. Relevant data are needed to target basic research, to identify the potential for acute and long-term complications, and to plan therapeutic interventions. The following specific aims will be addressed in non-diabetic schizophrenia patients treated with atypical antipsychotics who will be randomized to open label treatment with either valproate or no adjuvant. Evaluations are performed at baseline and 3 months of treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
Diabetes, Metabolic

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
164 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
50% of participants will receive placebo
Arm Title
Experimental
Arm Type
Experimental
Arm Description
50% of participants will receive Depakote ER
Intervention Type
Drug
Intervention Name(s)
Valproate
Other Intervention Name(s)
Depakote ER
Intervention Description
Depakote ER 500 mg to 3000 mg taken every night
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo given at same frequency as Valproate
Primary Outcome Measure Information:
Title
Change From Baseline in Total Body Fat Composition Using Dual Energy X-ray Absorptiometry at 12 Weeks
Description
Change in body composition (total body fat) was assessed using dual energy x-ray absorptiometry
Time Frame
Measured at baseline and Week 12
Title
Effects of Medication on Insulin Secretion at Skeletal Muscle (Glucose Disposal)
Time Frame
Measured at baseline and Week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meets DSM-IV criteria for schizophrenia, any type, treated with the same antipsychotic for at least 6 months No antipsychotic medication dose changes for 1 month, and no other medication changes for 1 month prior to study entry Exclusion Criteria: Meets DSM-IV criteria for substance abuse within 3 months of study entry Involuntary legal status (as per Missouri law) Any serious medical disorder that may confound the assessment of relevant biologic measures or diagnosis, including: significant organ system dysfunction, metabolic diseases, type 1 or 2 diabetes mellitus, pregnancy, endocrine disease, coagulopathy, anemia, or acute infection Currently taking more than one antipsychotic medication Currently taking prescription medications (except certain psychotropic medications as discussed below), including oral contraceptive pills, any glucose lowering agent, lipid lowering agent, exogenous testosterone, recombinant human growth hormone, or any other endocrine agent that might confound substrate metabolism
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dan W. Haupt, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11806485
Citation
Haupt DW, Newcomer JW. Hyperglycemia and antipsychotic medications. J Clin Psychiatry. 2001;62 Suppl 27:15-26; discussion 40-1.
Results Reference
background
Links:
URL
http://www.psychiatry.wustl.edu/
Description
Click here for the Washington University Department of Psychiatry

Learn more about this trial

Determining Metabolic Effects of Valproate and Antipsychotic Therapy

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