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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03118193
Other study ID # PHAO16-WEH/BIORESA
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 16, 2017
Est. completion date January 12, 2021

Study information

Verified date April 2021
Source University Hospital, Tours
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

According to the WHO, major depressive disorders have become the second worldwide cause of disability. Treatment, long-term medication, leads to frequent resistance (up to 40%). Establishing a cerebral molecular signature of depression is not feasible in humans (need for cerebral samples). The alternative is to use peripheral biological samples (blood, urine, saliva). Metabolomic is the integrated and quantitative study of all the metabolites of a biological system. This aims to define the metabolic status of an organism for a particular condition. Metabolites are derived from biological extracts (cells, tissues, serum, plasma, urine, etc.) and are detected by: - liquid or gas chromatography coupled to mass spectrometry (LC-MS, GC-MS), - proton nuclear magnetic resonance (1 H-NMR). The biomarkers resulting from these studies have become important diagnostic criteria, measured objectively and evaluated as indicators of a normal or pathological state, or even predictors of treatment efficacy. This approach allows the discovery of biomarkers that best describe the status of a disease for better understanding and are usable in a context of individualized medicine, with effects on clinical practice and management.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date January 12, 2021
Est. primary completion date January 12, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - between 18-60 years-old - major depressive disorder, confirmed by Mini International Neuropsychiatric Interview (MINI) - no bipolar disorder or schizophrenia, confirmed by MINI - no neurological dementia disease - able to perform olfactive tests, i.e. no anosmia and/or allergy to odors - score MADRS (Montgomery AsbergDepression Rating Scale) >20 - no antidepressant treatment during 14 days before inclusion - informed written consent - affiliation to a social security system Exclusion Criteria: - patient who don't want any antidepressant treatment for this depressive episode - legal incapacity and/or any circumstances making the person unable to understand the trial features, purposes or consequences - participating to drug clinical study or in exclusion period of clinical study because of previous participation - pregnant woman

Study Design


Related Conditions & MeSH terms


Intervention

Other:
olfactive tests
olfactive tests: odor identification, odor discrimination and olfactory threshold
Biological:
blood test
one sample of 4mL
Collection of faeces
Collection of faeces by patient at home - optional
Device:
Tissue Pulsatility imaging
Ultrasound exploration of brain pulsatility - optional

Locations

Country Name City State
France CHU Tours Tours

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Tours

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary metabolic print of blood Metabolome of blood 2 months
Secondary olfactive identification Olfactive response: odor identification 2 months
Secondary olfactive discrimination Olfactive response: odor discrimination 2 months
Secondary Olfactory threshold Olfactive response: olfactory threshold 2 months
Secondary Microbiote of faeces Bacteria of faeces 2 months
Secondary Maximal measures of brain pulsatility Maximal brain pulsatility 2 months
Secondary Mean measures of brain pulsatility Mean brain pulsatility 2 months
Secondary Metabolic print of faces Metabolome of faeces 2 months
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