Curcumin Addition to Antipsychotic Treatment in Chronic Schizophrenia Patients
关键词
抽象
描述
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.
日期
| 最后验证: | 12/31/2018 |
| 首次提交: | 11/17/2014 |
| 提交的预估入学人数: | 11/19/2014 |
| 首次发布: | 11/23/2014 |
| 上次提交的更新: | 01/13/2019 |
| 最近更新发布: | 01/14/2019 |
| 实际学习开始日期: | 12/31/2014 |
| 预计主要完成日期: | 12/31/2016 |
| 预计完成日期: | 04/30/2017 |
状况或疾病
干预/治疗
Drug: Curcumin
Drug: placebo
相
手臂组
| 臂 | 干预/治疗 |
|---|---|
| Active Comparator: curcumin curcumin 3 g/day for 6 months | |
| Placebo Comparator: placebo curcumin 3 g/day for 6 months |
资格标准
| 有资格学习的年龄 | 18 Years 至 18 Years |
| 有资格学习的性别 | All |
| 接受健康志愿者 | 是 |
| 标准 | 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 |
结果
主要结果指标
1. Positive and Negative Symptoms Scale (PANSS) [up to 24 weeks]
次要成果指标
1. Clinical Global Impression - Improvement (CGI-I) [up to 24 weeks]
2. Clinical Global Impression - Severity of Adverse Events (CGI-SAE) [up to 24 weeks]
3. Calgary Depression Scale for Schizophrenia (CDSS) [up to 24 weeks]
