search
Back to results

FEcal Microbiota Transplantation

Primary Purpose

Depression in Schizophrenia

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Experimental drug
Sponsored by
Assistance Publique Hopitaux De Marseille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Depression in Schizophrenia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

  • history of lifetime FMT
  • History of gut surgery

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Other

    Arm Label

    Clinical trial

    Arm Description

    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.

    Outcomes

    Primary Outcome Measures

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

    Secondary Outcome Measures

    Full Information

    First Posted
    June 20, 2019
    Last Updated
    June 26, 2019
    Sponsor
    Assistance Publique Hopitaux De Marseille
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT04001439
    Brief Title
    FEcal Microbiota Transplantation
    Official Title
    FEcal Microbiota Transplantation for MAjor Depression in Schizophrenia (FEMADSZ)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    December 1, 2019 (Anticipated)
    Primary Completion Date
    February 1, 2020 (Anticipated)
    Study Completion Date
    December 31, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Assistance Publique Hopitaux De Marseille

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    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.
    Detailed Description
    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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Depression in Schizophrenia

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    All patients will receive 30 microbiota capsules in take proceded by bowel lavage by 4 liters macrogo solution.
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    3088 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Clinical trial
    Arm Type
    Other
    Arm Description
    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.
    Intervention Type
    Drug
    Intervention Name(s)
    Experimental drug
    Intervention Description
    All patients will recive 30 microbiota capsules intake preceded by bowel lavage by 4 liters macrogol solution. the capsules are developed by the services of JC Lagier.
    Primary Outcome Measure Information:
    Title
    myoglobin concentration
    Description
    the primary outcome for efficacy will be the improvement of depressive symtoms
    Time Frame
    2 moths

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: patients aged 18 to 65 years with the current diagnosis of shizophrenia Exclusion Criteria: history of lifetime FMT History of gut surgery

    12. IPD Sharing Statement

    Learn more about this trial

    FEcal Microbiota Transplantation

    We'll reach out to this number within 24 hrs