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临床试验/NCT04001439
NCT04001439Unknown不适用

FEcal Microbiota Transplantation for MAjor Depression in Schizophrenia (FEMADSZ)

Assistance Publique Hopitaux De Marseille0 个研究点目标入组 3,088 人开始时间: 2019年12月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
3,088
主要终点
myoglobin concentration

研究概览

简要总结

The primary objective will be to evaluate effectiveness, safety and acceptability of FMT on depressive symptoms at 2 months follow-up in SZ patients with resistant MD.

详细描述

Background. Major Depression (MD) will move into the first place of cause of the global burden of disease by 2030. Conventional treatments (antidepressants) are only partly effective with frequent side effects. More specifically, MD is underdiagnosed and undertreated in schizophrenia (SZ) despite its high impact on prognosis and quality of life in SZ patients. Even when treated, 44% of the patients remain major depressed under conventional antidepressants.

FEMADSZ makes the hypothesis that this is due to the fact that the source of MD relies outside the brain, in the gut microbiota. The associations between microbiota disturbances are now well demonstrated in rodent models (>60 studies) and indirect data in humans clearly suggest that the microbiota hypothesis of MD is the most promising track in psychiatry. The primary objective will be to evaluate effectiveness, safety and acceptability of FMT on depressive symptoms at 2 months follow-up in SZ patients with resistant MD. Methods: This is a pilot, single-arm, prospective, open-label proof-of-concept trial, including SZ patients with resistant MD. Fifteen patients will be enrolled and administered a Fecal Microbiota Transplantation. The main outcome measure will be depressive score at 2 months, adverse events and acceptability. Each patient will receive a FDG-PET scan, a routine blood draw and a metagenomic microbiota analysis before and after intervention. Expected results. This pilot study will help determining the effectiveness of FMT and the neurobiologic and microbiologic mechanisms associated with response to treatment.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients aged 18 to 65 years
  • with the current diagnosis of shizophrenia

排除标准

  • history of lifetime FMT
  • History of gut surgery

研究组 & 干预措施

Clinical trial

Other

the study design is an open-label, single-arm propective clinical trial. In this proof-of-concept study we will assess feasibility safety and potential efficacy of an intervention of FMT in SZ subjects with MD.

干预措施: Experimental drug (Drug)

结局指标

主要结局

myoglobin concentration

时间窗: 2 moths

the primary outcome for efficacy will be the improvement of depressive symtoms

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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