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Addition of Ondansetron to Ongoing Antipsychotic Treatment for Schizophrenia

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Ondansetron followed by placebo
Placebo followed by Ondansetron
Sponsored by
University of Colorado, Denver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Schizophrenia, Ondansetron, P50 sensory gating, Evoked potentials, 5-HT3 receptors, Atypical antipsychotics

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Meets DSM-IV criteria for schizophrenia Stable, chronic schizophrenia Currently taking atypical medications Use of effective form of contraception throughout study Exclusion Criteria: History of any alcohol or drug abuse within 3 months of study start date Any other major neurological disorders History of or current head trauma Any medical conditions affecting the central nervous system Current epilepsy, asthma, migraine headache, previous myocardial infarction, stroke, diabetes, hypertension, narrow angle glaucoma, or neuromuscular illnesses Pregnant

Sites / Locations

  • Denver VAMC

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Ondansetron followed by placebo

Placebo followed by Ondansetron

Arm Description

Participants will take ondansetron then placebo plus an atypical antipsychotic drug

Participants will take placebo then ondansetron plus an atypical antipsychotic drug

Outcomes

Primary Outcome Measures

P50 Sensory Gating
P50 Sensory Gating as measured by evoked potentials (response to stimuli, in this case, clicking sounds).The P50 potential was identified and measured using a computer algorithm. The amplitude of the P50 test wave was divided by the amplitude of the P50 conditioning wave, expressed as a percentage: the P50 ratio. Lower P50 ratios represent better outcomes.
Cognitive Testing

Secondary Outcome Measures

Full Information

First Posted
September 6, 2005
Last Updated
July 20, 2021
Sponsor
University of Colorado, Denver
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00149734
Brief Title
Addition of Ondansetron to Ongoing Antipsychotic Treatment for Schizophrenia
Official Title
Atypical Antipsychotics and P50 Sensory Gating
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
May 2010 (Actual)
Study Completion Date
May 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will examine the effects of ondansetron on auditory nerve activity in people with schizophrenia who are being treated with new antipsychotics.
Detailed Description
Schizophrenia is a devastating brain disorder. Most people with schizophrenia have difficulty filtering out unimportant auditory information. They have an inability to appropriately inhibit, or gate, sensory information that enters the ear. Standard treatments do not address this problem. When the drug ondansetron is taken in addition to typical antipsychotic drugs, P50 auditory gating improves. However, ondansetron has not been used with some of the newer, atypical antipsychotic drugs. This study will evaluate the effect of combining ondansetron with newer, atypical antipsychotic drugs on P50 auditory gating. Participants in this double-blind study will be randomly assigned to receive either ondansetron or placebo for 3 months. Upon completion of the first 3 months, participants will be crossed over to receive the other treatment for an additional 3 months. All participants will also take an atypical antipsychotic drug, including olanzapine, quetiapine, or aripiprazole. Auditory gating will be assessed using computerized cognitive testing and functional magnetic resonance imaging (fMRI) at baseline and Months 3 and 6. Vital signs and evoked potentials will be assessed at Weeks 1, 3, and 6. Clinical symptoms and cognitive abilities will also be evaluated to determine the effectiveness of ondansetron.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
Schizophrenia, Ondansetron, P50 sensory gating, Evoked potentials, 5-HT3 receptors, Atypical antipsychotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ondansetron followed by placebo
Arm Type
Experimental
Arm Description
Participants will take ondansetron then placebo plus an atypical antipsychotic drug
Arm Title
Placebo followed by Ondansetron
Arm Type
Experimental
Arm Description
Participants will take placebo then ondansetron plus an atypical antipsychotic drug
Intervention Type
Drug
Intervention Name(s)
Ondansetron followed by placebo
Other Intervention Name(s)
Zofran, Zuplenz
Intervention Description
Participants will take 16mg of ondansetron daily for the first three months followed by 3 months of placebo. An atypical antipsychotic drug (olanzapine,quetiapine, or aripiprazole) will also be taken throughout the 6 months treatment period.
Intervention Type
Drug
Intervention Name(s)
Placebo followed by Ondansetron
Other Intervention Name(s)
Zofran, Zuplenz
Intervention Description
Participants will take placebo daily for the first three months followed by 3 months of 16mg of ondansetron daily. An atypical antipsychotic drug (olanzapine,quetiapine, or aripiprazole) will also be taken throughout the 6 months treatment period.
Primary Outcome Measure Information:
Title
P50 Sensory Gating
Description
P50 Sensory Gating as measured by evoked potentials (response to stimuli, in this case, clicking sounds).The P50 potential was identified and measured using a computer algorithm. The amplitude of the P50 test wave was divided by the amplitude of the P50 conditioning wave, expressed as a percentage: the P50 ratio. Lower P50 ratios represent better outcomes.
Time Frame
Up to 3 hours
Title
Cognitive Testing
Time Frame
Measured at Months 3 and 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meets DSM-IV criteria for schizophrenia Stable, chronic schizophrenia Currently taking atypical medications Use of effective form of contraception throughout study Exclusion Criteria: History of any alcohol or drug abuse within 3 months of study start date Any other major neurological disorders History of or current head trauma Any medical conditions affecting the central nervous system Current epilepsy, asthma, migraine headache, previous myocardial infarction, stroke, diabetes, hypertension, narrow angle glaucoma, or neuromuscular illnesses Pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lawrence E. Adler, MD
Organizational Affiliation
University of Colorado Health Sciences Center, VISN19 MIRECC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Denver VAMC
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
15677607
Citation
Adler LE, Cawthra EM, Donovan KA, Harris JG, Nagamoto HT, Olincy A, Waldo MC. Improved p50 auditory gating with ondansetron in medicated schizophrenia patients. Am J Psychiatry. 2005 Feb;162(2):386-8. doi: 10.1176/appi.ajp.162.2.386.
Results Reference
background
PubMed Identifier
15465979
Citation
Adler LE, Olincy A, Cawthra EM, McRae KA, Harris JG, Nagamoto HT, Waldo MC, Hall MH, Bowles A, Woodward L, Ross RG, Freedman R. Varied effects of atypical neuroleptics on P50 auditory gating in schizophrenia patients. Am J Psychiatry. 2004 Oct;161(10):1822-8. doi: 10.1176/ajp.161.10.1822.
Results Reference
background

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Addition of Ondansetron to Ongoing Antipsychotic Treatment for Schizophrenia

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