Effect of Atypical Antipsychotic Drugs Olanzapine and Amisulpride on Glucose Metabolism
Primary Purpose
Schizophrenia, Diabetes, Insulin Resistance
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Glucose clamp technique
Amisulpride
Olanzapine
Placebo
Sponsored by
About this trial
This is an interventional basic science trial for Schizophrenia focused on measuring schizophrenia, olanzapine, atypical antipsychotic drugs, amisulpride, diabetes, insulin resistance, insulin secretion, glucose, euglycemic hyperinsulinemic clamp, hyperglycemic clamp
Eligibility Criteria
Inclusion Criteria:
- healthy male volunteers
- written informed consent
Exclusion Criteria:
- BMI > 30 kg/m²
- Diabetes mellitus
- Hypertension
- Treatment with drugs interfering with lipid or glucose metabolism (e.g. statins, oral antidiabetic drugs, glucocorticoids)
- History of seizures
Sites / Locations
- Central Institute of Mental Health
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Experimental
Placebo Comparator
Arm Label
Amisulpride
Olanzapine
Placebo
Arm Description
Single dose of amisulpride 200 mg p.o. given at 8:00 a.m.
Single dose of olanzapine 10 mg p.o. given at 8:00 a.m.
Placebo capsules are given at 8:00 a.m. Procedures are performed as described above.
Outcomes
Primary Outcome Measures
insulin sensitivity
m-value during euglycemic glucose clamp (glucose infusion rate divided by time and body weight)
Secondary Outcome Measures
pancratic c-peptide secretion
C-peptide measured 4 times during hyperglycemic clamp period at time 0 min (prior to glucose bolus), 5 min, 10 min and 60 min after glucose bolus
Full Information
NCT ID
NCT01160991
First Posted
July 9, 2010
Last Updated
August 2, 2010
Sponsor
Central Institute of Mental Health, Mannheim
Collaborators
Sanofi
1. Study Identification
Unique Protocol Identification Number
NCT01160991
Brief Title
Effect of Atypical Antipsychotic Drugs Olanzapine and Amisulpride on Glucose Metabolism
Official Title
Effects of the Serotonin 2A Receptor on Insulin Sensitivity and Secretion: a Double-blind Controlled Comparison of Olanzapine vs. Amisulpride:
Study Type
Interventional
2. Study Status
Record Verification Date
August 2010
Overall Recruitment Status
Completed
Study Start Date
May 2004 (undefined)
Primary Completion Date
October 2006 (Actual)
Study Completion Date
October 2006 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Central Institute of Mental Health, Mannheim
Collaborators
Sanofi
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients suffering from schizophrenia have a high risk to become obese and develop diabetes. Risk of obesity is particularly high with some newer schizophrenia drugs, such as clozapine or olanzapine. These drugs are called atypical drugs and exert their action in part by occupying receptors for serotonin, particularly the 5HT2A receptor subtype. This receptor may also interfere with glucose metabolism and insulin action. The purpose of this study is to compare an atypical antipsychotic drugs, olanzapine, which acts by occupying the 5HT2A receptor, to another antipsychotic drug, amisulpride, which mainly acts through the dopamine pathway. Healthy volunteers are recruited and asked to take a single dose of each drug and of placebo on separate days. Then, a combined glucose clamp study will be performed in order to test the effects of these drugs on insulin sensitivity and insulin secretion.
Detailed Description
10 male healthy volunteers are recruited. After informed consent, they are admitted to the study ward at 10:00 p.m. prior to the study day and kept fasting until the next morning. At 8:00 a.m. they receive their study medication (olanzapine, amisulpride or placebo). Subsequently, measurements of insulin sensitivity and insulin secretion are performed by euglycemic hyperinsulinemic clamp technique followed by hyperglycemic clamp.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Diabetes, Insulin Resistance
Keywords
schizophrenia, olanzapine, atypical antipsychotic drugs, amisulpride, diabetes, insulin resistance, insulin secretion, glucose, euglycemic hyperinsulinemic clamp, hyperglycemic clamp
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Amisulpride
Arm Type
Active Comparator
Arm Description
Single dose of amisulpride 200 mg p.o. given at 8:00 a.m.
Arm Title
Olanzapine
Arm Type
Experimental
Arm Description
Single dose of olanzapine 10 mg p.o. given at 8:00 a.m.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo capsules are given at 8:00 a.m. Procedures are performed as described above.
Intervention Type
Procedure
Intervention Name(s)
Glucose clamp technique
Intervention Description
euglycemic hyperinsulinemic clamp with target blood glucose of 90 mg/dl (5 mmol/l), followed by hyperglycemic clamp, target blood glucose of 180 mg/dl (10 mmol/l) for measurement of insulin sensitivity and insulin secretion
Intervention Type
Drug
Intervention Name(s)
Amisulpride
Intervention Description
Single dose of amisulpride 200 mg p.o. given at 8:00 a.m.
Intervention Type
Drug
Intervention Name(s)
Olanzapine
Intervention Description
Single dose of olanzapine 10 mg p.o. given at 8:00 a.m.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo capsules are given at 8:00 a.m.
Primary Outcome Measure Information:
Title
insulin sensitivity
Description
m-value during euglycemic glucose clamp (glucose infusion rate divided by time and body weight)
Time Frame
90 thru 120 min after application of study drug
Secondary Outcome Measure Information:
Title
pancratic c-peptide secretion
Description
C-peptide measured 4 times during hyperglycemic clamp period at time 0 min (prior to glucose bolus), 5 min, 10 min and 60 min after glucose bolus
Time Frame
120 thru 180 minutes after administration of study drug
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
healthy male volunteers
written informed consent
Exclusion Criteria:
BMI > 30 kg/m²
Diabetes mellitus
Hypertension
Treatment with drugs interfering with lipid or glucose metabolism (e.g. statins, oral antidiabetic drugs, glucocorticoids)
History of seizures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Kopf, M.D.
Organizational Affiliation
Central Institute of Mental Health, Mannheim
Official's Role
Principal Investigator
Facility Information:
Facility Name
Central Institute of Mental Health
City
Mannheim
ZIP/Postal Code
68159
Country
Germany
12. IPD Sharing Statement
Learn more about this trial
Effect of Atypical Antipsychotic Drugs Olanzapine and Amisulpride on Glucose Metabolism
We'll reach out to this number within 24 hrs