FEcal Microbiota Transplantation
Primary Purpose
Depression in Schizophrenia
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Experimental drug
Sponsored by
About this trial
This is an interventional other trial for Depression in Schizophrenia
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
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
NCT ID
NCT04001439
First Posted
June 20, 2019
Last Updated
June 26, 2019
Sponsor
Assistance Publique Hopitaux De Marseille
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
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