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Antipsychotic Augmentation With L-Dopa

Augmentation of Antipsychotics With L-Dopa (Sinemet)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01636037
Enrollment
13
Registered
2012-07-10
Start date
2012-09-30
Completion date
2016-01-31
Last updated
2016-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizophrenia

Keywords

schizophrenia, negative symptoms, deficit syndrome, SANS, Sinemet, L-dopa, levodopa, carbidopa, augmentation, antipsychotics

Brief summary

Dopamine, a chemical in the brain, has been linked to schizophrenia for a number of years. More recently, there is evidence that certain areas affected in schizophrenia (e.g. motivation, cognition) may reflect too little dopamine, whereas symptoms like hallucinations and delusions have been linked to too much dopamine. This study is designed to evaluate the safety, tolerability, and efficacy of giving L-dopa (Sinemet) to see if it will improve those symptoms related to too little dopamine. L-dopa has been approved for other medical conditions (e.g. Parkinson's disease) and works to increase levels of dopamine. The investigators are linking this study with neuroimaging (fMRI) which will allows us to link any changes the investigators might find in clinical symptoms with changes in the brain. This information can prove useful in better understanding the mechanisms that account for these symptoms, as well as possible new treatments. At present , treatments for these other symptoms that seem important in functional measures of outcome (i.e. deficit symptoms, including amotivation; cognitive symptoms) in schizophrenia have not proven particularly effective. It is hoped that L-dopa may provide a treatment that is more effective; going forward, this information would also be useful in drug development and future lines of investigation. 1. L-dopa will prove effective in improving deficit (also called 'primary negative' e.g. amotivation) and cognitive symptoms in schizophrenia. 2. It will be well tolerated and not increase risk of psychotic symptoms when administered in conjunction with their regular antipsychotic medications.

Detailed description

Pharmacological (and non-pharmacological) strategies that may significantly improve the negative and cognitive symptoms of schizophrenia represent a critical unmet therapeutic need. There is wide acceptance of the notion that both negative and cognitive symptoms are best understood as features of hypo- rather than hyperdopaminergic activity. The primary negative and cognitive symptoms appear central to schizophrenia and predate the neurodevelopmental changes that subsequently give rise to the hyperdopaminergic state underlying positive symptoms. In using L-Dopa specifically, we avoid the abuse potential of agents such as the psychostimulants, or perturbations in pharmacological action as a function of dose, as observed with dopamine agonists. Further, more recent neuroimaging studies have provided in vivo evidence in keeping with the underlying rationale. First, imaging studies have demonstrated that L-dopa induces shifts in activity in both cortical and subcortical structures linked to reward, affect and cognition. Along similar lines, L-dopa-induced changes have been associated with improvement in motivation, cognitive tasks, and affect.

Interventions

DRUGlevodopa/carbidopa (generic version of Sinemet)

Oral levodopa 900mg daily as tolerated.

Sponsors

Centre for Addiction and Mental Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* SCID-confirmed (Structured Clinical Interview for DSM-IV Axis I Disorders) diagnosis of schizophrenia * ages 18-55

Exclusion criteria

* history of substance abuse or dependence within 3 months; (ii) positive urine drug screen * history or evidence of any disorder that might adversely influence cognitive measures (e.g. mental retardation) * presence of serious neurological or general medical condition (e.g., Parkinson's disease, cardiac arrhythmia, epilepsy) * clinical or laboratory evidence of uncompensated cardiovascular, endocrine, hematologic, hepatic, pulmonary (including bronchial asthma), or renal disease, narrow-angle glaucoma, malignant melanoma * pregnancy/nursing or women of child-bearing age not on regular contraceptive therapy (effects of L-dopa unknown)

Design outcomes

Primary

MeasureTime frame
SANS - Schedule for the Assessment of Negative Symptoms8 weeks

Secondary

MeasureTime frameDescription
BPRS - Brief Psychotic Rating Scale8 weeks
SAPS - Schedule for the Assessment of Positive Symptoms8 weeks
NIMH-MATRICS Brief Negative Symptoms Scale8 weeks
CGI-S - Clinical Global Impression - Severity Scale8 weeks
QLS - Quality of Life Scale8 weeks
CDS - Calgary Depression Scale8 weeks
SAS - Simpson Angus Scale for Extrapyramidal Symptoms8 weeks
BARS - Barnes Akathisia Rating Scales8 weeks
MATRICS-Consensus Cognitive Battery8 weeks
UKU - Udvalg for Kliniske Undersogelses8 weeksMeasures General Side Effects
LUNSERS - Liverpool University Neuroleptic Side-Effect Rating Scale8 weeks
BIS-11 - Barrett Impulsivity Scale8 weeks
Y-BOCS - Yale-Brown Obsessive Compulsive Scale8 weeks
DAI - Drug Attitude Inventory8 weeks
fMRI - Functional Magnetic Resonance Imaging8 weeksChanges in Regional Brain Activity
SWN - Subjective Well-Being on Neuroleptics Scale8 weeks
AIMS - Abnormal Involuntary Movement Scale8 weeks

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026