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Telmisartan as an Adjunctive Treatment for Metabolic Problems in Patients With Schizophrenia
This study is currently recruiting participants.
Verified by Massachusetts General Hospital, September 2009
First Received: September 18, 2009   Last Updated: September 21, 2009   History of Changes
Sponsor: Massachusetts General Hospital
Collaborator: National Institutes of Health (NIH)
Information provided by: Massachusetts General Hospital
ClinicalTrials.gov Identifier: NCT00981526
  Purpose

This is a 12-week, randomized, double-blinded, placebo-controlled trial of telmisartan 80 mg/day as an adjunctive to clozapine or olanzapine therapy, in 70 schizophrenia subjects to examine telmisartan's effect on glucose metabolism, weight, food intake, resting energy expenditure, and body composition. In addition, the study will examine insulin's effects on psychopathology and cognition.

Potential subjects will be identified by their clinicians at the Freedom Trail Clinic, or Massachusetts General Hospital. A total of 70 subjects will be enrolled.


Condition Intervention Phase
Schizophrenia
Schizoaffective Disorder
 Drug: Telmisartan
Drug: Placebo
 Phase IV

Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment
Official Title: Telmisartan as an Adjunctive Treatment for Metabolic Problems in Patients With Schizophrenia

Resource links provided by NLM:

MedlinePlus related topics: Schizophrenia
Drug Information available for: Telmisartan
U.S. FDA Resources

Further study details as provided by Massachusetts General Hospital:

Primary Outcome Measures:
  • Metabolism, weight, food intake, energy, and body composition [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Cognition and psychopathology [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment: 70
Study Start Date: March 2009
Estimated Study Completion Date: December 2010
Estimated Primary Completion Date: December 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
A: Experimental: Experimental Drug: Telmisartan
Telmisartan 40mg/day, or placebo for the first 2 weeks. Telmisartan 80mg/day, or placebo for the next 10 weeks.
B: Placebo: Placebo Comparator Drug: Placebo
Telmisartan 40mg/day, or placebo for the first 2 weeks. Telmisartan 80mg/day, or placebo for the next 10 weeks.

Detailed Description:

The specific aims include:

Primary Aims:

  1. Examine the efficacy of telmisartan added to regular doses of clozapine or olanzapine in improving insulin resistance.
  2. Examine the efficacy of telmisartan in reducing fasting triglycerides.

Secondary Aims:

  1. Examine the effects of telmisartan on negative symptoms, positive symptoms, and cognitive function.
  2. Examine the efficacy of telmisartan in improving glucose metabolism as measured by glucose effectiveness (SG) and the acute insulin response to glucose (AIRG).
  3. Examine telmisartan's effects on lipids, body composition, waist circumference, and waist/hip ratio.
  4. Examine telmisartan's effects on weight, food intake and resting energy expenditure.
  5. Characterize the relationships between changes in CRP, IL-6, and changes in fasting insulin and glucose, SI, SG, and AIRG from FSIVGTT.
  6. Characterize the relationships between changes in fasting insulin and glucose, SI, SG, and AIRG from FSIVGTT, CRP, IL-6, and changes in negative symptoms, positive symptoms and cognitive function.
  7. Examine telmisartan's effects on inflammatory biomarkers including C-reactive protein (CRP) and interleukin 6 (IL-6).
  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Age 18-65 years
  2. Diagnosis of schizophrenia, any subtype or schizoaffective disorder, any subtype
  3. Treatment with clozapine or olanzapine for at least 6 months
  4. Stable dose of antipsychotic agent for at least one month
  5. Well establish compliance with out-patient medications
  6. Females subjects will be eligible to participate in the study if they are of non-childbearing potential or of child-bearing potential and willing to practice appropriate birth control methods (complete abstinence from sexual intercourse, female sterilization, sterilization of male partner, implants of levonorgestrel, injectable progestogen, oral contraceptives, intrauterine devices, or double barrier methods of contraception using spermicide with either a condom or diaphragm) during the study.

Exclusion Criteria:

  1. Inability to provide informed consent
  2. Current substance abuse
  3. Psychiatrically unstable
  4. Significant medical illness including severe cardiovascular, hepatic, renal disease
  5. Current insulin treatment of diabetes
  6. History of immunosuppression
  7. Current or recent radiation or chemotherapy treatment for cancer
  8. Chronic use of steroids
  9. Pregnancy or breast feeding
  10. Use of diuretics, digoxin, warfarin because the possible drug-drug interaction of telmisartan
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00981526

Contacts
Contact: Karina Tsatourian, Ph.D. 617-912-7837 ktsatourian@partners.org
Contact: Ju Hyung Park, BA 617-912-7848 jpark24@partners.org

Locations
United States, Massachusetts
Massachusetts General Hospital Recruiting
Boston, Massachusetts, United States, 02116
Principal Investigator: Xiaduo Fan, M.D.            
Sponsors and Collaborators
Massachusetts General Hospital
National Institutes of Health (NIH)
Investigators
Principal Investigator: Xiaoduo Fan, M.D. Massachusetts General Hospital
  More Information

No publications provided

Responsible Party: Massachusetts General Hospital ( Xiaoduo Fan )
Study ID Numbers: 2008-P-000790
Study First Received: September 18, 2009
Last Updated: September 21, 2009
ClinicalTrials.gov Identifier: NCT00981526     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Massachusetts General Hospital:
Schizophrenia
Cognition
Metabolism
Antipsychotics
Psychopathology

Additional relevant MeSH terms:
Angiotensin II Type 1 Receptor Blockers
Schizophrenia
Molecular Mechanisms of Pharmacological Action
Mental Disorders
Angiotensin-Converting Enzyme Inhibitors
Enzyme Inhibitors
 Psychotic Disorders
Telmisartan
Pharmacologic Actions
Schizophrenia and Disorders with Psychotic Features
Protease Inhibitors

ClinicalTrials.gov processed this record on February 08, 2010



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