Clinical Trials Directory

Trials / Completed

CompletedNCT01139463

Study of Blood Lactate Levels in Patients Treated With Antipsychotics

Blood Lactate Levels in Patients Treated With Typical or Atypical Antipsychotics

Status
Completed
Phase
Study type
Observational
Enrollment
60 (actual)
Sponsor
University of Split · Academic / Other
Sex
Male
Age
20 Years – 50 Years
Healthy volunteers
Not accepted

Summary

Blood lactate levels in patients receiving typical or atypical antipsychotics have not been described in the literature. The goal of this study is to assess the dynamics of lactate levels in the blood from typical or atypical antipsychotics not confounded by prior antipsychotic treatments, the investigators conducted a prospective study of lactate levels in patients receiving antipsychotic medication. The investigators hypothesized that 6 months of treatment with haloperidol or olanzapine would result in a change in blood lactate levels and extrapyramidal side effects.

Detailed description

The aim of this study was to compare the blood lactate levels in patients receiving typical or atypical antipsychotics. Subjects included sixty patients with psychotic disorder were assigned to treatment for 6 months with haloperidol (typical antipsychotic), N=30 or olanzapine (atypical antipsychotic), N=30. Blood lactate levels, other metabolic parameters, and scores on the extrapyramidal symptom rating scale (ESRS) were assessed.

Conditions

Interventions

TypeNameDescription
DRUGHaloperidol or olanzapineHaloperidol tablet - 5 mg twice daily (morning and evening) by mouth Olanzapine tablet - 5 mg twice daily (morning and evening) by mouth

Timeline

Start date
2008-06-01
Primary completion
2009-10-01
Completion
2009-10-01
First posted
2010-06-08
Last updated
2010-06-08

Locations

1 site across 1 country: Croatia

Source: ClinicalTrials.gov record NCT01139463. Inclusion in this directory is not an endorsement.