The study aims to evaluate the contribution of a multi-targeted microbiotherapy at 12 weeks in depressed-patients in a situation of failure of a 1st line of antidepressant treatment and treated in add-on with a 2nd antidepressant, venlafaxine.
Depression is the most common psychiatric illness and has major personal, societal and economic consequences. Increase in the disease prevalence is significantly associated with certain somatic pathologies, including metabolic diseases and functional intestinal disorders. From a therapeutic point of view, approximately 2/3 patients are not in remission after first-line antidepressant treatment. Moreover, 20 to 30% patients resist at all the therapeutic strategies classically proposed in this indication. The identification of new therapeutic strategies is therefore a major challenge, especially for patients with chronic depression resistant to standard treatments. Various research studies have shown the involvement of inflammatory mechanisms in depression. Thus, the increase in the disease prevalence is significantly associated with certain somatic pathologies, in particular metabolic diseases, a certain number of which are linked to abnormalities of the intestinal microbiota. In this context, the use of probiotics is interesting because some have antidepressant effects, anti-inflammatory and metabolic properties. However, even if a few studies have shown an antidepressant effect of probiotics with improvement of biological markers of inflammation, it seems that the use of probiotics alone is not sufficient for lasting results on depressive symptoms. The PROMOOD clinical research project fits into this context. We propose to carry out a multicenter clinical study with the product developed by GYNOV (GynMDD® multitarget compound with 3 active ingredients: an amino acid (L-glutamine), an ingredient purified from a plant extract (Cavacurmine) and a probiotic (Lactobacillus rhamnosus GG). In a preclinical study carried out at the CNRS on 144 mice, a synergy of action between these 3 ingredients was demonstrated on the anxio-depressive systems, resulting in an improvement far greater than the expected effect of composition and comparable to a reference injectable antidepressant (clomipramine). In theses context, the microbiotherapy proposed in this project is very original because: * a multi-target approach targeting several mechanisms of action: intestinal permeability, glutamine/glutamate/GABA cycle, insulin resistance, immunomodulation, oxidative stress; * prospect of an optimization/simplification of care; * It is very acceptable for patients both from the point of view of tolerance and from the economic point of view. With a phase II, prospective, multicenter design, this study aims to evaluate the contribution and the tolerance of a multi-targeted microbiotherapy in addition to venlafaxine, in a second-line antidepressant treatment. The treatment will be delivered during 12 weeks. Baseline measures will be compared to those obtained during the treatement administration (every week) and after the treatment administration (every week for the next 12 weeks).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
92
multi-target microbiotherapy add-on venlafaxine
placebo add-on venlafaxine
Emmanuel HAFFEN
Besançon, France
RECRUITINGCentre Hospitalier Spécialisé Charles Perrens
Bordeaux, France
NOT_YET_RECRUITINGCHU de Clermont-Ferrand
Clermont-Ferrand, France
NOT_YET_RECRUITINGChange from Baseline Quick Inventory of Depressive Symptomatology (QIDS-C16) at 12 weeks
The QIDS-C16 is a 16-item scale that is clinician-rated; it is designed to assess the severity of depressive symptoms. The QIDS-C16 total score ranges from 0-27. Scores ranging from 0 to 10 correspond with no to mild depression, while scores \>/= 11 correspond to moderate to severe depression. A negative change indicates improvement in the subject's depression, and a positive change indicates a worsening of the subject's depression.
Time frame: baseline (Day 0), Week 12 (W12) post-treatment
Change from Severity of depressive symptoms evaluated by the clinician
The QIDS-C16 was derived from specified items in the IDS-C30, clinician-rated scale to assess the severity of a participant's depressive symptoms. Total scores range from 0-27, with a score of 0 indicating no depression and a score of 27 indicating the most severe depression. Negative change from baseline values indicate improvement in the severity of depression.
Time frame: baseline (Day 0), at the end of therapy (week 12 (W12)
Change from Severity of depressive symptoms evaluated by the patient
Score achieved on the validated self-reported (QIDS-SR16) evaluating the severity of depressive symptoms. QIDS-SR-16 is a standard questionnaire "The Quick Inventory of Depressive Symptomatology" (16-Item) (Self-Report). This covers questions on falling asleep, sleep during the night, waking up , sleeping too much, feeling sad ,appetite, weight, concentration , how they view themselves, thoughts of death and suicide, general interests, energy levels, feeling slowed down , feeling restless.
Time frame: baseline (Day 0), at the end of therapy (week 12 (W12)
Evaluation of treatment observance
A treament observance book was complied by patient during the 12 weeks of therapy
Time frame: baseline (Day 0), at the end of therapy (week 12 (W12)
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Hôpital Henri Mondor / APHP
Créteil, France
Change from Health related Quality of Life (HrQoL)
HrQOL will be assessed using health status measures of the EuroQuality of Life Five Dimensions (EQ-5D-5L)
Time frame: baseline (Day 0), at the end of therapy (week 12 (W12)
Change from anxiety
anxiety assessed using Brief Anxiety Scale of Tyrer (BAS)
Time frame: baseline (Day 0), at the end ot therapy (week 12 (W12)
Change from digestive health
digestive evaluation assessed by digestive health scale, scale developped by gastroenterlogists (https://www.worldgastroenterology.org/search?cx=005474681532606414716%3AWMX-367025812\&cof=FORID%3A9\&ie=UTF-8\&q=digestive+health+evaluation)
Time frame: baseline (Day 0), at the end ot therapy (week 12 (W12)
Change from serum Inflammatory biological markers
inflammatory inflammatory levels (CRP, Il-1b, Il-6 and TNF-a) in blood samples
Time frame: baseline (Day 0), at the end ot therapy (week 12 (W12)
Change from Biological markers of intestinal dysbiosis
zonulin and serobank levels in blood samples
Time frame: baseline (Day 0), at the end ot therapy (week 12 (W12)
Change from Metagenomic shotgun sequencing of gut microbiota
preforming metagenomic shotgun sequencing of fecal DNA to determine the changes in the intestinal microbiota composition, diversity and functionality
Time frame: baseline (Day 0), at the end ot therapy (week 12 (W12)