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临床试验/NCT03304457
NCT03304457已完成4 期

Effect of Lurasidone Vs Olanzapine on Neurotrophic Biomarkers and Cardiometabolic Parameters in First Episode Untreated Schizophrenia: A Randomized, Open Label, Active Controlled Study

All India Institute of Medical Sciences, Bhubaneswar1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2017年8月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
Serum brain derived neurotrophic factor (BDNF)

研究概览

简要总结

Schizophrenia (SCZ) is a chronic, severe and disabling mental disorder with unclear etiology and pathophysiology concerned with neuro-developmental,neurodegenerative abnormalities and cognitive impairmentslinked to behavioural changes.According to neurotrophic hypothesis, the changes result due to the abnormal regulation of neurotrophic factor, especially the decreased serum brain derived neurotrophic factor (BDNF) validated by several meta-analyses. However, the regulation of nerve growth factor (NGF) in SCZ remains unclear because of the inconsistent findings from the previous clinical studies.

Lurasidone is a novel antipsychotic drug approved for adult SCZ and for affective symptomatology & cognitive deficits. Principal advantages over some other second-generation antipsychotics are its highly favourable metabolic profile and once daily dosing regimen. Some of the studies indicate that risperidone, olanzapine, clozapine & aripiprazole might not alter BDNF levels, at least within 8 weeks of treatment.While other two studies with olanzapine suggest that BDNF might influence the response to monotherapy in SCZ patients.All these previous studies are non-conclusive & contradictory to each other which draw our attention for doing the research further to reach a conclusive result about the effect of olanzapine and lurasidone on neurotrophic biomarkers in SCZ.

详细描述

Schizophrenia (SCZ) is a chronic, severe and disabling mental disorder with unclear aetiology and pathophysiology concerned with neuro-developmental,neurodegenerative abnormalities and cognitive impairments linked to behavioural changes.According to neurotrophic hypothesis, the changes result due to the abnormal regulation of neurotrophic factor, especially the decreased serum brain derived neurotrophic factor (BDNF) validated by several meta-analyses. However, the regulation of nerve growth factor (NGF) in SCZ remains unclear because of the inconsistent findings from the previous clinical studies.

Lurasidone is a novel antipsychotic drug approved for adult SCZ and for affective symptomatology & cognitive deficits. Principal advantages over some other second-generation antipsychotics are its highly favourable metabolic profile and once daily dosing regimen. Some of the studies indicate that risperidone, olanzapine, clozapine & aripiprazole might not alter BDNF levels, at least within 8 weeks of treatment.While other two studies with olanzapine suggest that BDNF might influence the response to monotherapy in SCZ patients.All these previous studies are non-conclusive & contradictory to each other which draw our attention for doing the research further to reach a conclusive result about the effect of olanzapine and lurasidone on neurotrophic biomarkers in SCZ.

Most of the antipsychotic drugs prescribed for SCZ are based on the dopamine hypothesis. In recent times, neurotrophic hypothesis gained importance in the pathophysiology of SCZ. So, our study may enable psychiatrist to choose a better antipsychotic drug having effect on both dopamine as well as neurotrophic factors. Previously there were no studies on effect of lurasidone on neurotrophic factors in SCZ & also there was no head-on comparison of lurasidone and olanzapine

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
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •All treatment naive patients clinically diagnosed first episode of SCZ according to ICD-10
  • •Patients of either sex with age range 18-45 years
  • •Treatment naïve patients

排除标准

  • •Other Psychotic spectrum disorders (F21- F29)
  • •Highly agitated/ violent/ suicidal patients who need immediate treatment
  • •Patients with comorbid substance abuse except Nicotine use or history of organicity
  • •Patients with known history of diabetes mellitus, hypertension or any long standing significant medical illness/ significant neurological impairment/ clinical observable mental retardation
  • •Pregnant and nursing women

研究组 & 干预措施

Olanzapine

Active Comparator

Olanzapine will be prescribed at a dose of 10mg once daily orally for 6 weeks

干预措施: Olanzapine (Drug)

Lurasidone

Experimental

Lurasidone will be prescribed at a dose of 80mg/day once daily orally for 6 weeks

干预措施: Lurasidone (Drug)

结局指标

主要结局

Serum brain derived neurotrophic factor (BDNF)

时间窗: 6 weeks

the change in serum level of BDNF from baseline after treatment with lurasidone or olanzapine

次要结局

  • Serum Neurotrophin 3 (NT3)(6 weeks)
  • Serum Insulin(6 weeks)
  • Fasting blood sugar(6 weeks)
  • Low Density Lipoprotein (LDL)(6 week)
  • serum nerve growth factor (NGF)(6 weeks)
  • Social and occupational functioning assessment scale (SOFAS)(6 weeks)
  • PANSS score(6 weeks)
  • High Density Lipoprotein (HDL)(6 week)
  • Serum Triglyceride(6 weeks)
  • Glycosylated Hemoglobin (HbA1c)(6 weeks)
  • Very Low Density Lipoprotein (VLDL)(6 week)
  • LDL/HDL ratio(6 weeks)
  • Serum hsCRP(6 weeks)

研究者

发起方
All India Institute of Medical Sciences, Bhubaneswar
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Monalisa Jena, M.D.

Assistant Professor

All India Institute of Medical Sciences, Bhubaneswar

研究点 (1)

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