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Curcumin Addition to Antipsychotic Treatment in Chronic Schizophrenia Patients

Primary Purpose

Chronic Schizophrenia

Status
Completed
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
Curcumin
placebo
Sponsored by
Beersheva Mental Health Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Schizophrenia focused on measuring curcumin; schizophrenia; neuroprotection

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-60 years, male or female
  • DSM-IV criteria for schizophrenia.
  • Ability and willingness to sign informed consent for participation in the study
  • SANS (Scale of Negative Symptoms of Schizophrenia ) > 30 points
  • Fixed antipsychotic dosages at least 3 months
  • Steady mental state of patients at least 3 months

Exclusion Criteria:

  • Current substance use disorder except nicotine dependence
  • Regular use of NSAID (non-steroidal anti-inflammatory drugs)
  • Cancer history
  • Untreated or severe hypertension
  • Poorly controlled diabetes mellitus Type I or Type II
  • Chronic liver & gallbladder diseases
  • Recent GERD (Gastroesophageal Reflux Disorder)
  • Neurological disorders: epilepsy, stroke
  • Hamilton Depression Scale Hamilton Depression Rating Scale (HAM-D-17 item) > 24 points
  • Patients with a known hypersensitivity to curcumin
  • Pregnant women or a woman who intends to become pregnant

Sites / Locations

  • Beersheva Mental Health Center
  • Tirat Carmel Mental Health Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

curcumin

placebo

Arm Description

curcumin 3 g/day for 6 months

curcumin 3 g/day for 6 months

Outcomes

Primary Outcome Measures

Positive and Negative Symptoms Scale (PANSS)
baseline and every week 4 up to 24 weeks

Secondary Outcome Measures

Clinical Global Impression - Improvement (CGI-I)
baseline and every week 4 up to 24 weeks
Clinical Global Impression - Severity of Adverse Events (CGI-SAE)
baseline and every week 4 up to 24 weeks
Calgary Depression Scale for Schizophrenia (CDSS)
baseline and every week 4 up to 24 weeks

Full Information

First Posted
November 18, 2014
Last Updated
January 14, 2019
Sponsor
Beersheva Mental Health Center
Collaborators
Tirat Carmel Mental Health Center
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1. Study Identification

Unique Protocol Identification Number
NCT02298985
Brief Title
Curcumin Addition to Antipsychotic Treatment in Chronic Schizophrenia Patients
Official Title
Curcumin as add-on to Antipsychotic Treatment in Chronic Schizophrenia Patients: A Randomized, Double-Blind, Placebo-controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
January 2015 (Actual)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
May 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beersheva Mental Health Center
Collaborators
Tirat Carmel Mental Health Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Schizophrenia is still remained one of the disabling disorders despite progress in treatment of mental disturbances. Ten to thirty percents of patients have a little or no benefit from treatment with all kinds of antipsychotics using adequate dosages and duration. Treatment of these patients has remained a persistent public health problem since medication-resistant patients are often highly symptomatic. Curcumin is one of the main curcuminoids isolated from this perennial herb. It possesses a variety of pharmacological activities, including anti-inflammatory, antiproliferative, antioxidant, and neuroprotective effects and crosses the blood-brain barrier. The purpose of our suggested study is to examine the efficacy of curcumin as add-on the conventional antipsychotic psychopharmacotherapy in chronic schizophrenia patients.
Detailed Description
Study Design This is a 24-week, randomized, double-blind, placebo-controlled investigation of 40 chronic schizophrenia patients. Participants Forty patients will be drawn from the patient population of Be'er Sheva Mental Health Center. Recruitment period will last over 2 years. Patients will be required to have a primary diagnosis of chronic schizophrenia as defined in DSM-IV with predominantly persistent negative signs. The study will commence only after approval by the local Institutional Ethics Review Board ("Helsinki Committee"). Only willing subjects and able to provide written informed consent, after receiving a comprehensive explanation of the study procedures, will be included in the study. Confidentially will be ensured by means of a number coding system, and all completed research forms will be stored in secure areas. Procedure Patients will continue receiving their regular antipsychotic medication. The dose will be kept constant for at least 3 months prior to entry and throughout the study period. Curcumin is provided as Curcumin Forte ® (Solgar Israel SupHerb). Circumin capsules are supplied as an 1000 mg soft gelatin capsule for three daily oral administration with meals. At entry patients will receive curcuma capsules (3000 mg/day, three capsules) or placebo in identical capsules in a randomized, double blind mode for 24 weeks: 20 patients will receive curcumin, and 20 patients - placebo. Participants will be assessed at baseline and after 4, 8, 12, 16 and 24 weeks of treatment. In a case of treatment discontinuation for 24-week of the trial, patients will be followed until end of study period. Outcome variables will be evaluated by scoring the severity of symptoms (positive, negative, and etc.), and side effects. In addition, liver function tests and a blood cell count will be monitored at baseline and during the study. For analyzing the results, within-subject pre- and post-treatment responses would be subject to statistical procedures to evaluate whether curcumin can ameliorate the persistent negative symptoms in schizophrenia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Schizophrenia
Keywords
curcumin; schizophrenia; neuroprotection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
38 (Actual)

8. Arms, Groups, and Interventions

Arm Title
curcumin
Arm Type
Active Comparator
Arm Description
curcumin 3 g/day for 6 months
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
curcumin 3 g/day for 6 months
Intervention Type
Drug
Intervention Name(s)
Curcumin
Other Intervention Name(s)
placebo, regular antipsychotic medication
Intervention Description
3 g/day (3 capsules/day) for 6 months
Intervention Type
Drug
Intervention Name(s)
placebo
Other Intervention Name(s)
curcumin, regular antipsychotic medication
Intervention Description
3 g/day (3 capsules/day) for 6 months
Primary Outcome Measure Information:
Title
Positive and Negative Symptoms Scale (PANSS)
Description
baseline and every week 4 up to 24 weeks
Time Frame
up to 24 weeks
Secondary Outcome Measure Information:
Title
Clinical Global Impression - Improvement (CGI-I)
Description
baseline and every week 4 up to 24 weeks
Time Frame
up to 24 weeks
Title
Clinical Global Impression - Severity of Adverse Events (CGI-SAE)
Description
baseline and every week 4 up to 24 weeks
Time Frame
up to 24 weeks
Title
Calgary Depression Scale for Schizophrenia (CDSS)
Description
baseline and every week 4 up to 24 weeks
Time Frame
up to 24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-60 years, male or female DSM-IV criteria for schizophrenia. Ability and willingness to sign informed consent for participation in the study SANS (Scale of Negative Symptoms of Schizophrenia ) > 30 points Fixed antipsychotic dosages at least 3 months Steady mental state of patients at least 3 months Exclusion Criteria: Current substance use disorder except nicotine dependence Regular use of NSAID (non-steroidal anti-inflammatory drugs) Cancer history Untreated or severe hypertension Poorly controlled diabetes mellitus Type I or Type II Chronic liver & gallbladder diseases Recent GERD (Gastroesophageal Reflux Disorder) Neurological disorders: epilepsy, stroke Hamilton Depression Scale Hamilton Depression Rating Scale (HAM-D-17 item) > 24 points Patients with a known hypersensitivity to curcumin Pregnant women or a woman who intends to become pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vladimir Lerner, MD, PhD
Organizational Affiliation
Ben-Gurion University of the Negev
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beersheva Mental Health Center
City
Beersheva
Country
Israel
Facility Name
Tirat Carmel Mental Health Center
City
Tirat Carmel
ZIP/Postal Code
84170
Country
Israel

12. IPD Sharing Statement

Citations:
PubMed Identifier
31045590
Citation
Miodownik C, Lerner V, Kudkaeva N, Lerner PP, Pashinian A, Bersudsky Y, Eliyahu R, Kreinin A, Bergman J. Curcumin as Add-On to Antipsychotic Treatment in Patients With Chronic Schizophrenia: A Randomized, Double-Blind, Placebo-Controlled Study. Clin Neuropharmacol. 2019 Jul/Aug;42(4):117-122. doi: 10.1097/WNF.0000000000000344.
Results Reference
derived

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Curcumin Addition to Antipsychotic Treatment in Chronic Schizophrenia Patients

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