A Pilot Trial of Curcumin Effects on Cognition in Schizophrenia



Status:Terminated
Conditions:Schizophrenia, Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - 65
Updated:1/24/2018
Start Date:February 11, 2016
End Date:August 24, 2017

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This is an 8-week randomized, double-blind, placebo-controlled, parallel, fixed-dose pilot
clinical trial of curcumin for the treatment of cognitive impairment in schizophrenia.The
primary aim of this pilot trial is to provide an effect size estimate for the efficacy of
curcumin in improving cognitive functioning in schizophrenia. Secondary goals are to
determine the effect of curcumin over time on negative and positive symptoms, in association
with inflammatory markers.

This is an 8-week randomized, double-blind, placebo-controlled, parallel, fixed-dose pilot
clinical trial of curcumin for the treatment of cognitive impairment in schizophrenia.
Cognitive impairment and persistent negative symptoms are the core dimensions of
schizophrenia; however current antipsychotic treatment fails to address this issue. Evidence
suggests cognitive impairment is not only limited to patients with late-stage schizophrenia.
High rates of cognitive impairment in patients with first episode psychosis indicate that
cognitive impairment is not solely a consequence of long-term antipsychotic treatment, but
rather is an enduring problem over the course of schizophrenia. Likewise, negative symptoms
persist throughout its entire course, and are associated with poor overall functioning.
Currently, there are no pharmacological agents that specifically aim to treat cognitive
functioning and persistent negative symptoms; therefore, there is growing interest in the
development of effective treatments for this unmet need.

The primary aim of this pilot trial is to provide an effect size estimate for the efficacy of
curcumin in improving cognitive functioning in schizophrenia. Secondary goals are to
determine the effect of curcumin over time on negative and positive symptoms, in association
with inflammatory markers. Eligible participants will be randomized to curcumin (n=20) or
placebo (n=20) in a 1:1 ratio. A commercially available surface-controlled water soluble form
of 600mg curcumin (10% formulation) or matching placebo capsules will be administered three
times a day for a total of 8 weeks.

Inclusion criteria:

1. 18 - 65 years of age

2. English speaking

3. Diagnostic and Statistical Manual- IV diagnosis of schizophrenia or schizoaffective
disorder based on Structured Clinical Interview for Diagnostic and Statistical
Manual-IV (SCID)

4. Symptomatic stability confirmed by clinical staff in the 8 weeks prior to the study

5. No changes in antipsychotic medication within the last 8 weeks

6. No change in antipsychotic dose in in last 4 weeks.

Exclusion criteria are:

1. Unable to provide informed consent

2. Diagnostic and Statistical Manual-IV (DSM-IV) diagnosis of alcohol/substance
dependence

3. Recent history of gastrointestinal bleeding or ulceration

4. Recent history of gallstones and/or bile duct obstruction

5. Significant uncontrolled systemic illness (e.g. chronic renal failure, chronic liver
disease, poorly controlled diabetes, poorly controlled congestive heart failure,
chronic infectious disease, chronic autoimmune disease)

6. Known intolerance to turmeric, curcumin, or curry

7. Pregnancy or breast-feeding

8. Current use of anti-platelet, anti-coagulant, glucocorticoid, immunosuppressants

9. Daily use of non-steroidal anti-inflammatory use.
We found this trial at
1
site
New Haven, Connecticut 06508
Principal Investigator: Cenk Tek, MD
Phone: 203-974-7317
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from
New Haven, CT
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