Curcumin Addition to Antipsychotic Treatment in Chronic Schizophrenia Patients

Chronic Schizophrenia Clinical Trial

Official title:

Curcumin as add-on to Antipsychotic Treatment in Chronic Schizophrenia Patients: A Randomized, Double-Blind, Placebo-controlled Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02298985
• Other study ID #: VLJB-14
• Status: Completed
• Phase: Phase 4
• Start date: January 2015
• Est. completion date: May 2017

Study information

• Verified date: January 2019
• Source: Beersheva Mental Health Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 38
• Est. completion date: May 2017
• Est. primary completion date: January 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

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

Related Conditions & MeSH terms

• Chronic Schizophrenia
• Schizophrenia

Intervention

Drug:
• Curcumin
3 g/day (3 capsules/day) for 6 months
• placebo
3 g/day (3 capsules/day) for 6 months

Locations

Country	Name	City	State
Israel	Beersheva Mental Health Center	Beersheva
Israel	Tirat Carmel Mental Health Center	Tirat Carmel

Sponsors (2)

Lead Sponsor	Collaborator
Beersheva Mental Health Center	Tirat Carmel Mental Health Center

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Positive and Negative Symptoms Scale (PANSS)	baseline and every week 4 up to 24 weeks	up to 24 weeks
Secondary	Clinical Global Impression - Improvement (CGI-I)	baseline and every week 4 up to 24 weeks	up to 24 weeks
Secondary	Clinical Global Impression - Severity of Adverse Events (CGI-SAE)	baseline and every week 4 up to 24 weeks	up to 24 weeks
Secondary	Calgary Depression Scale for Schizophrenia (CDSS)	baseline and every week 4 up to 24 weeks	up to 24 weeks