EUCTR2010-023983-42-RO进行中(未招募)1 期
A randomized trial administering Raloxifene vs. Placebo as add-on to antipsychotics in post menopausal patients with schizophrenia or schizoaffecive disorder
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •1.Post menopausal females: Post menopausal defined as: Women 45 years of age and older with no vaginal bleeding for at least 2 years prior to randomization, and both serum estradiol <73 pmol/L (20 pg/mL) and FSH >30 IU/L (30 mIU/mL).
- •2.45-65 years old
- •3.Willing and able to provide informed consent, after the nature of the study has been fully explained.
- •4.Current DSM-IV-TR diagnosis of schizophrenia or schizoaffective disorder as confirmed by modified SCID and having had at least 2 prior schizophrenic episodes, or continually ill for at least 6 months.
- •5.Symptoms: 4 (moderate) or above on CGI-S and ? 4 (moderate) score on two of the following four PANSS items: delusions, hallucinatory behaviors, conceptual disorganization or suspiciousness/ persecution, and/or a total PANSS negative symptoms score of 18.
- •6.Must be on any antipsychotic drug, for at least 2 weeks prior to the baseline visit, at doses within the PORT criteria, whenever possible. Patients receiving higher doses will have their records reviewed to insure that the dose is required and, if possible, will be stabilized on a lower dose prior to study entry.
- •7.Inpatients or outpatients. Inpatients will be randomized 3 days or more after admission.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1.Unwilling or unable, in the opinion of the Investigator, to comply with study instructions
- •2.Women of child bearing potential.
- •3.Women who have amenorrhea due to causes other than natural or surgical menopause i.e. eating disorders or exercise
- •4.Unstable medical disease (malignancy, poorly controlled diabetes, active ischemic cardiac disease, or cardiomyopathy, serious pulmonary disease, kidney disease, impaired liver functioning.
- •5.Patients treated with cholestyramine, warfarin or concurrent systemic estrogen therapy
- •6.Likely allergy or sensitivity to raloxifene.
- •7.At significant risk of committing suicide, or in the opinion of the Investigator, currently is at imminent risk of suicide or harming others.
- •8.Patients with a current DSM-IV substance or alcohol abuse. Patients with a history of and/or current recreational use of cannabinoids or alcohol, and/or patients who smoke cigarettes can be included.
- •9.Concurrent delirium, mental retardation, drug-induced psychosis, or history of brain trauma.
研究者
相似试验
Unknown
3 期
Raloxifene in Treatment of Schizophrenia and Schizoaffective DisorderSchizophreniaSchizoaffective DisorderNCT01280305Sheba Medical Center200
已完成
不适用
clinical trial on the efficacy of Raloxifene on disease activity in Rheumatoid ArthritisRheumatoid Arthritis.Rheumatoid arthritis, unspecifiedIRCT2015052022334N1Research Chancellor of Mashhad University of Medical Sciences40
已完成
3 期
Comparison of Raloxifene Hydrochloride and Placebo in the Treatment of Postmenopausal Women With OsteoporosisOsteoporosis, PostmenopausalNCT00670319Eli Lilly and Company7,705
已完成
不适用
A randomized controlled trial of venlafaxine versus placebo for depression amongst persons with lymphoma or leukaemiaISRCTN51232664Department of Health (UK)
已完成
不适用
A randomized controlled trial of sorafenib versus 5-FU arterial infusion and interferon therapy (FAIT) for advanced hepatocellular carcinomahepatocellular carcinomaJPRN-UMIN000002401Department of Hepatology, Kyoundo Hospital140
