Salsalate for Insulin Resistance in Schizophrenia
Primary Purpose
Schizophrenia, Insulin Resistance
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
salsalate
Sponsored by
About this trial
This is an interventional treatment trial for Schizophrenia focused on measuring schizophrenia, salsalate, obesity
Eligibility Criteria
Inclusion Criteria:
- DSM-IV TR diagnosis of schizophrenia or schizoaffective disorder
- Body Mass Index (BMI) greater than or equal to 27 kg/m2
- Participant will be judged to be clinically stable
- Participants will be treated with the same antipsychotic for at least 90 days and will have received a constant therapeutic dose for at least 20 days prior to study entry. There will not be any restriction on the type of antipsychotic with which the participant is treated.
- Participants must be judged competent to participate in the informed consent process and provide voluntary informed consent.
Exclusion Criteria:
- Individuals with aspirin allergy.
- Individuals with pre-existing tinnitus.
- Individual with anemia or thrombocytopenia.
- Individuals with ongoing infections.
- Individuals with history of autoimmune disease.
- Individuals with peptic ulcer disease or gastritis.
- Individuals with weight loss greater than 5% over the past 6 months.
- Individuals currently taking immunosuppressive drugs including corticosteroids.
- Individuals taking anti-diabetic agents.
- Individuals taking non-steroidal anti-inflammatory agents (other than low dose aspirin).
- Individuals with organic brain disorder; mental retardation; or medical conditions whose pathology or treatment would alter the presentation or treatment of schizophrenia or significantly increase the risk associated with the proposed treatment protocol.
- Pregnant females.
- Individuals who meet DSM-IV TR criteria for alcohol or substance dependence (except nicotine) within the last 6 months.
- Individuals who meet DSM-IV TR criteria for alcohol or substance abuse (except nicotine) within the last month.
Sites / Locations
- Baltimore VA Medical Center
- Maryland Psychiatric Research Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
salsalate
Arm Description
Salsalate will be administered in two divided doses of 2grams in the morning and 2 grams in the evening. Salsalate will be administered for 6 weeks. If a participant is not able to tolerate the target dose of 4 grams per day then 500 mg reductions will be made in a stepwise fashion until a tolerated dose or a minimum dose of 2 grams per day is reached.
Outcomes
Primary Outcome Measures
Side Effects of Salsalate
This Measure is reporting the number of participants with side effects as reported on the Side Effect Checklist used to monitor common medication side effects.
Secondary Outcome Measures
Full Information
NCT ID
NCT01182727
First Posted
August 13, 2010
Last Updated
March 1, 2022
Sponsor
University of Maryland, Baltimore
Collaborators
US Department of Veterans Affairs
1. Study Identification
Unique Protocol Identification Number
NCT01182727
Brief Title
Salsalate for Insulin Resistance in Schizophrenia
Official Title
Salsalate for the Treatment of Insulin Resistance in People With Schizophrenia
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
August 2010 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
December 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Maryland, Baltimore
Collaborators
US Department of Veterans Affairs
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Being obese is a common problem for people with schizophrenia. People with schizophrenia are more likely to be overweight compared to the general population. Being overweight is a major risk factor for developing type II diabetes. Approximately 15% of people with schizophrenia have type II diabetes. People with type II diabetes have problems with their body's insulin. Insulin is a hormone produced by the body to control blood sugar level. Obesity and type II diabetes are strong risk factors for heart disease. In type II diabetes the body does not respond to insulin correctly. Obesity, type II diabetes, and insulin resistance are all common states of inflammation. Inflammation is a reaction by the body to irritation, injury, or infection.
Salicylates are non-steroidal anti-inflammatory drugs. Aspirin is an example of a salicylate. These drugs work by decreasing the level of inflammation in the body. Salicylates have been shown to decrease inflammation and improve the body's response to insulin. Improving the body's response to insulin and decreasing inflammation could possibly reduce the risk of developing type II diabetes. Salicylates have been known for years to be effective for the treatment of diabetes. Salicylates increase the body's response to insulin causing blood sugar levels to decrease. Many salicylate drugs have side effects including stomach irritation and increased risk of bleeding. The drug for this study is called salsalate and is different from other salicylates. Salsalate has a lower bleeding risk than aspirin. Salsalate has been used to treat arthritis and has been shown to be safe.
There have been no studies using salsalate in people with schizophrenia. The purpose of this study is to gain experience in the use of salsalate in people with schizophrenia. The study would be a pilot study to obtain preliminary data. The study would be a 6-week study where everyone in the study would receive the drug salsalate. The participants in the study will have tests of baseline symptoms of schizophrenia, a physical exam, EKG (to check heart function), and a side effect checklist for possible side effects from salsalate. The study will also have some blood drawn to measure blood sugar levels, insulin levels, and inflammatory markers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Insulin Resistance
Keywords
schizophrenia, salsalate, obesity
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)
8. Arms, Groups, and Interventions
Arm Title
salsalate
Arm Type
Experimental
Arm Description
Salsalate will be administered in two divided doses of 2grams in the morning and 2 grams in the evening. Salsalate will be administered for 6 weeks. If a participant is not able to tolerate the target dose of 4 grams per day then 500 mg reductions will be made in a stepwise fashion until a tolerated dose or a minimum dose of 2 grams per day is reached.
Intervention Type
Drug
Intervention Name(s)
salsalate
Intervention Description
Salsalate will be administered in 500 mg tablets. Salsalate will be administered in two divided doses of 2 grams in the morning and 2 grams in the evening. Salsalate will be administered for a total of 6 weeks. If a participant is not able to tolerate the target dose of 4 grams per day then 500 mg reductions will be made in a stepwise fashion until tolerated or a minimum dose of 2 grams per day is achieved.
Primary Outcome Measure Information:
Title
Side Effects of Salsalate
Description
This Measure is reporting the number of participants with side effects as reported on the Side Effect Checklist used to monitor common medication side effects.
Time Frame
6 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
DSM-IV TR diagnosis of schizophrenia or schizoaffective disorder
Body Mass Index (BMI) greater than or equal to 27 kg/m2
Participant will be judged to be clinically stable
Participants will be treated with the same antipsychotic for at least 90 days and will have received a constant therapeutic dose for at least 20 days prior to study entry. There will not be any restriction on the type of antipsychotic with which the participant is treated.
Participants must be judged competent to participate in the informed consent process and provide voluntary informed consent.
Exclusion Criteria:
Individuals with aspirin allergy.
Individuals with pre-existing tinnitus.
Individual with anemia or thrombocytopenia.
Individuals with ongoing infections.
Individuals with history of autoimmune disease.
Individuals with peptic ulcer disease or gastritis.
Individuals with weight loss greater than 5% over the past 6 months.
Individuals currently taking immunosuppressive drugs including corticosteroids.
Individuals taking anti-diabetic agents.
Individuals taking non-steroidal anti-inflammatory agents (other than low dose aspirin).
Individuals with organic brain disorder; mental retardation; or medical conditions whose pathology or treatment would alter the presentation or treatment of schizophrenia or significantly increase the risk associated with the proposed treatment protocol.
Pregnant females.
Individuals who meet DSM-IV TR criteria for alcohol or substance dependence (except nicotine) within the last 6 months.
Individuals who meet DSM-IV TR criteria for alcohol or substance abuse (except nicotine) within the last month.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert W Buchanan, MD
Organizational Affiliation
University of Maryland School of Medicine Maryland Psychiatric Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Baltimore VA Medical Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
Facility Name
Maryland Psychiatric Research Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21228
Country
United States
12. IPD Sharing Statement
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Salsalate for Insulin Resistance in Schizophrenia
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