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Open-label Study of Curcumin C-3 Complex in Schizophrenia

Primary Purpose

Schizophrenia, Schizoaffective Disorder, Depression

Status
Completed
Phase
Phase 1
Locations
Puerto Rico
Study Type
Interventional
Intervention
Super-Curcumin
Sponsored by
Woodbury, Michel, M.D.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Curcumin, Epigenetics, Schizophrenia, Nitric Oxide synthetase, cognition, negative symptoms

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female:
  • DSMIV (Diagnostic Statistical Manual -TR version) Schizophrenia
  • Male or Female ,
  • age 18-65 yrs
  • SANS (Scale of Negative Symptoms of Schizophrenia ) > 30
  • Stable antipsychotic dosage at least 1 month

Exclusion Criteria:

  • Current Substance use Disorder except Nicotine dependence
  • Regular Use of NSAID (non-steroidal anti-inflammatory drugs)
  • cancer History
  • Recent myocardial infarction
  • Unstable angina,
  • untreated or severe hypertension
  • Poorly controlled diabetes mellitus Type I or Type II
  • Chronic liver & gallbladder diseases
  • Recent GERD (Gastroesophageal Reflux Disorder)
  • Pregnancy and breast-fed.
  • Allergic reaction to Curcumin
  • Neurological disorders: epilepsy, stroke
  • Hamilton Depression Scale Hamilton Depression Rating Scale( HAM-D-17 item) > 24 -

Sites / Locations

  • Dr. Michel Woodbury-Farina

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Supercurcumin

Arm Description

The study protocol stipulates that subjects diagnosed as DSM IV-TR (Diagnostic Statistical Manual IV-Transitional Revised) would be receiving either 1 gm Super-Curcumin@ capsule once daily or 4 gm Super-Curcumin@ once daily for a total of 16 weeks. Super-Curcumin@ in capsule form is a patented formulation of curcumin certified by Sabinsa Corp.NJ USA and produced by America's Finest Inc. 1 gm-capsule Super-Curcumin@ consist of 1 gm Curcumin C-3 complex and 5 mg of Bioperine.

Outcomes

Primary Outcome Measures

Negative Symptoms
PANSS (Positive and Negative Symptom scale). The PANSS has three subscales: 1.Positive symptoms Subscale: delusions, hallucinations , and bizarre behavior; 2.Negative symptoms Subscale: alogia, anhedonia, social withdrawal, lack of motivation 3.General psychopathology Subscale: social interactions, anxiety, sleep, energy level --------------------------------------------------------------------------------

Secondary Outcome Measures

Neurocognition measures
The CNS Vital Sign@ is a standardized computerized battery of neurocognitive tests to be administered by trained research personnel to measure neurocognitive domains of memory, attention, logical reasoning, visual-spatial function and executive function.
Positive symptoms
PANSS (Positive subscale) to measure the positive symptoms: hallucinations, delusions, bizzare behavior and disorganized thoughts
General psychopathology
The BPRS is a standardized psychiatric rating scales to measure symptoms of general psychopathology, depression, anxiety, psychosis and somatic symptoms.

Full Information

First Posted
June 4, 2013
Last Updated
June 9, 2013
Sponsor
Woodbury, Michel, M.D.
Collaborators
Lawson Health Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01875822
Brief Title
Open-label Study of Curcumin C-3 Complex in Schizophrenia
Official Title
Open Label Study of Curcumin C-3 Complex, the Prototypal Epigenetic Modulator, as an Augmentation Strategy to Antipsychotic Therapy,for Improving Negative Symptoms and Cognition in Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
October 2011 (Actual)
Study Completion Date
May 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Woodbury, Michel, M.D.
Collaborators
Lawson Health Research Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Current evidence suggests that schizophrenia as a serious and complex psychiatric disorder, continues to challenge mental health professionals in their search for better treatment options in the community. In the present study, the investigators hypothesized that in patients diagnosed as schizophrenia, adjunct treatment with Curry extract from the plant labeled by botanists as Curcuma Longata, formulated as Super-Curcumin@ , would bring about :1)positive behavioral changes in areas of socialization, emotional well-being, verbal communication and motivation; 2)improvement in measures of memory. Throughout the study, the proprietary product, Super-Curcumin@ consisting of Curcumin C-3 complex combined with the black pepper extract Bioperine to boost the effects of Curcumin. The study was developed to examine whether Curcumin's interaction with the two major signal pathways in the brain regulating brain-behavior: the epigenetic signal (histone modification) and the anti-inflammatory signal (inducible nitric oxide synthetase)in preclinical models is translated to beneficial effects in the treatment of schizophrenia.
Detailed Description
Detailed Description: The overall objective of the study was to evaluate whether the standardized proprietary formulation of curcumin [Super Curcumin@ :C-3 Complex@ with Bioperine@) manufactured by American Finest Inc. NJ USA ] extracted from the curry plant (Curcuma Longata) , can improve the negative symptoms and cognitive impairments in patients diagnosed as schizophrenia and to determine the response rate in negative symptoms at 16 weeks. Response rate was defined as the positive change of minimum 30% or higher from baseline to the score measured at 16 weeks. Negative symptoms refer to the cluster of symptoms of apathy, alogia, blunted affect and lack of motivation affecting severely the ways the individual functions in the community at large. In the study, the investigators proposed to test the hypothesize that Super curcumin@ is efficacious and safe when combined with standard antipsychotic drugs in the cohort of patients diagnosed as schizophrenia. Throughout the study, the proprietary product(Super curcumin@) was used. Supercurcumin@ consisted of the primary medicinally active ingredient, Curcumin C-3 Complex, in combination with Bioperine@, the metabolic enhancer extracted from black pepper, in order to increase the systemic bioavailability of curcumin C-3 complex. For the oral formulation of Super- curcumin@: 1 gm-capsule has 1 gm of curcumin C-3 complex and 5 mg of Bioperine@ . The study protocol consisted of recruiting subjects with diagnosed as schizophrenia who would be receiving either 1 gm or 4 gm of Super-Curcumin@ given orally once daily for 16 weeks, on negative symptoms and cognition. For assessing the safety and tolerability of Supercurcumin@ , the study protocol required that the patients would be monitored regularly for vital signs:blood pressure, pulse,body weight, routine blood chemistry and comprehensive adverse events profile (Treatment Emergent Adverse Events checklist) including the AIMS (Abnormal Involuntary Movement Scale). At baseline and at regular intervals throughout the 16-week treatment period, standardized measures of negative and positive symptoms and neurocognition would be administered to examine the efficacy of Curcumin C-3 complex in schizophrenia. For analysing the results, within-subject pre- and post-treatment responses would be subject to statistical procedures to evaluate whether Super-Curcumin@ can ameliorate the persistent negative symptoms and cognitive deficits in schizophrenia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder, Depression
Keywords
Curcumin, Epigenetics, Schizophrenia, Nitric Oxide synthetase, cognition, negative symptoms

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
17 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Supercurcumin
Arm Type
Experimental
Arm Description
The study protocol stipulates that subjects diagnosed as DSM IV-TR (Diagnostic Statistical Manual IV-Transitional Revised) would be receiving either 1 gm Super-Curcumin@ capsule once daily or 4 gm Super-Curcumin@ once daily for a total of 16 weeks. Super-Curcumin@ in capsule form is a patented formulation of curcumin certified by Sabinsa Corp.NJ USA and produced by America's Finest Inc. 1 gm-capsule Super-Curcumin@ consist of 1 gm Curcumin C-3 complex and 5 mg of Bioperine.
Intervention Type
Dietary Supplement
Intervention Name(s)
Super-Curcumin
Other Intervention Name(s)
Super-Curcumin@: Curcumin C-3 complex and Bioperine
Intervention Description
The investigators are comparing the effects of the two dosages of Super-Curcumin@ capsules in the sample of subjects diagnosed as DSM IV-R schizophrenia
Primary Outcome Measure Information:
Title
Negative Symptoms
Description
PANSS (Positive and Negative Symptom scale). The PANSS has three subscales: 1.Positive symptoms Subscale: delusions, hallucinations , and bizarre behavior; 2.Negative symptoms Subscale: alogia, anhedonia, social withdrawal, lack of motivation 3.General psychopathology Subscale: social interactions, anxiety, sleep, energy level --------------------------------------------------------------------------------
Time Frame
Change from baseline Negative symptom at 16 weeks
Secondary Outcome Measure Information:
Title
Neurocognition measures
Description
The CNS Vital Sign@ is a standardized computerized battery of neurocognitive tests to be administered by trained research personnel to measure neurocognitive domains of memory, attention, logical reasoning, visual-spatial function and executive function.
Time Frame
Change from Baseline neurocognitive measures at 16 weeks
Title
Positive symptoms
Description
PANSS (Positive subscale) to measure the positive symptoms: hallucinations, delusions, bizzare behavior and disorganized thoughts
Time Frame
Change from Basline Positive symptoms at 16 weeks
Title
General psychopathology
Description
The BPRS is a standardized psychiatric rating scales to measure symptoms of general psychopathology, depression, anxiety, psychosis and somatic symptoms.
Time Frame
Change from baseline general psychopathology at 16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female: DSMIV (Diagnostic Statistical Manual -TR version) Schizophrenia Male or Female , age 18-65 yrs SANS (Scale of Negative Symptoms of Schizophrenia ) > 30 Stable antipsychotic dosage at least 1 month Exclusion Criteria: Current Substance use Disorder except Nicotine dependence Regular Use of NSAID (non-steroidal anti-inflammatory drugs) cancer History Recent myocardial infarction Unstable angina, untreated or severe hypertension Poorly controlled diabetes mellitus Type I or Type II Chronic liver & gallbladder diseases Recent GERD (Gastroesophageal Reflux Disorder) Pregnancy and breast-fed. Allergic reaction to Curcumin Neurological disorders: epilepsy, stroke Hamilton Depression Scale Hamilton Depression Rating Scale( HAM-D-17 item) > 24 -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michel Woodbury Farina, MD ABPN
Organizational Affiliation
University Puerto Rico San Juan PR (US)
Official's Role
Study Director
Facility Information:
Facility Name
Dr. Michel Woodbury-Farina
City
San Juan
ZIP/Postal Code
00918
Country
Puerto Rico

12. IPD Sharing Statement

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Open-label Study of Curcumin C-3 Complex in Schizophrenia

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