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临床试验/NCT01573637
NCT01573637已完成3 期

Six Month, Double Blind, Placebo-controlled Trial of the Efficacy of Raloxifene as an Adjuvant Treatment of the Negative Symptoms of Schizophrenia in Post-menopausal Women

Fundació Sant Joan de Déu3 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2011年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
78
试验地点
3
主要终点
To assess the efficacy of raloxifene (SERM - Selective Estrogen Receptor Modulator) as an adjuvant of antipsychotic treatment in the management of negative symptoms of schizophrenia in post-menopausal women.

研究概览

简要总结

The efficacy of raloxifene versus placebo was compared over a six-month period, as an adjuvant treatment of the negative symptoms of schizophrenia in a group of 80 post-menopausal women. The aim of the study is to analyze whether raloxifene has an effect on the positive and negative symptoms of schizophrenia, and on psychopathological symptoms in general, and on social and neuropsychological functioning, and to study the influence of genetic polymorphisms in treatment response.

详细描述

Several studies have found gender-related differences in the epidemiology, clinical presentation, clinical course and response to treatment of schizophrenic disorder(1,2). Findings relating to a lower frequency of schizophrenia in women, its later onset and less severe clinical course(3,4), have led to the appearance of the "estrogen hypothesis" of schizophrenia, which postulates that estrogen has a protective effect in women susceptible to this disease(5).

The estrogen hypothesis in relation to schizophrenia is based on several studies that showed that estrogen levels are significantly lower in schizophrenic women than in healthy women,(6) and that outbreaks or onset of the disease tend to coincide with stages of the menstrual cycle in which estrogen levels are the lowest(7,8).

Studies on experimental animals have shown that estrogen has a modulating effect on the brain dopaminergic system(9,10) and that it also affects serotoninergic activity(11). Estrogens also enhance neuronal regeneration and block mechanisms of neuronal death(12).

The discovery that estrogen has a modulatory effect on the dopaminergic system has encouraged some researchers to study the therapeutic use of estrogen in schizophrenic patients. Several double-blind clinical trials have shown that estrogens are effective at improving psychotic symptoms(13-15). These last studies analyzed the efficacy of estrogens after one and two months, and mainly in relation to positive symptoms, in patients with the acute illness. However, in older patients it is the severity of the negative, rather than the positive, symptoms that seems to be associated with a poorer cognitive and social function. Moreover, positive symptoms tend to be less severe with age, while negative symptoms tend to persist(16).

Regarding the possible use of estrogens to treat post-menopausal women with schizophrenia, Lindamer et al.,(17) studied the psychopathology of menopausal patients with schizophrenia and found that patients in hormone replacement therapy required lower doses of antipsychotic drugs and presented less negative symptoms, whereas no differences were found in response to treatment in relation to positive symptoms.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
45 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Raloxifene hydrochloride 60 mg

Experimental

Patients fulfilling inclusion criteria and those giving the general informed consent for the study will be randomly allocated to one of the two groups in the trial (placebo or raloxifene) in a 1:1 proportion and in blocks of 4 patients, using the random number tables designed for this purpose.

The dose of raloxifene hydrochloride administered will be 60 mg/day. Both placebo and the raloxifene will be administered over 6 months. Patients will take one single daily dose administered in the morning. Both drugs will be given orally in capsule form. The medication of each of the treatment groups (lactose as placebo, raloxifene) will be introduced into dark green gelatin capsules to guarantee the blinding.

干预措施: Raloxifene (Drug)

Lactosa (placebo)

Placebo Comparator

Patients fulfilling inclusion criteria and those giving the general informed consent for the study will be randomly allocated to one of the two groups in the trial (placebo or raloxifene) in a 1:1 proportion and in blocks of 4 patients, using the random number tables designed for this purpose.

The dose of raloxifene hydrochloride administered will be 60 mg/day. Both placebo and the raloxifene will be administered over 6 months. Patients will take one single daily dose administered in the morning. Both drugs will be given orally in capsule form. The medication of each of the treatment groups (lactose as placebo, raloxifene) will be introduced into dark green gelatin capsules to guarantee the blinding.

干预措施: Lactosa (placebo arm) (Drug)

结局指标

主要结局

To assess the efficacy of raloxifene (SERM - Selective Estrogen Receptor Modulator) as an adjuvant of antipsychotic treatment in the management of negative symptoms of schizophrenia in post-menopausal women.

时间窗: Change in score on the negative subscale of the PANSS from baseline to final assessment at week 24

The primary variable of efficacy will correspond to the change in score on the negative subscale of the PANSS from the start of treatment to the final assessment at 24 weeks. Patients will be considered to respond to treatment if the score in the negative subscale is at least 20% lower than at the start of treatment.

次要结局

  • To assess the efficacy of raloxifene as an adjuvant of antipsychotic treatment in the management of global symptoms of schizophrenia in postmenopausal women.(From baseline to week 24 (measurements at Baseline, weeks 4, 12, 24))
  • To assess the efficacy of raloxifene as an adjuvant of antipsychotic treatment in the global functioning of postmenopausal women with schizophrenia.(From baseline to week 24 (measurements at Baseline, weeks 4, 12, 24))
  • To assess the efficacy of raloxifene as an adjuvant of antipsychotic treatment in the neuropsychological functioning of post-menopausal women with schizophrenia(From baseline to week 24 (measurements at Baseline, week 12, week 24))
  • To control response to treatment as a function of genetic variants in the form of SNP (Single Nucleotide Polymorphisms) that patients present in the alfa (ESR1) and beta (ESR2) estrogenic receptor genes.(Blood sample collected at Baseline visit)
  • To assess the safety of the medication used in this patient population.(From Baseline to week 24)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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