Early Effects of Ketamine vs Placebo With Venlafaxine in Severe Depression Patients

Launched by ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS · Jul 15, 2024

Keywords

ClinConnect Summary

This clinical trial is investigating the effects of ketamine compared to a placebo (a substance with no therapeutic effect) when used alongside a medication called venlafaxine for patients experiencing severe depression. The goal is to see if ketamine can help these patients feel better more quickly, as traditional antidepressants often take weeks to show results. Participants will be adults aged 18 to 65 who are currently hospitalized due to a major depressive episode and have a specific score indicating the severity of their depression.

Eligible participants will receive either ketamine or placebo alongside venlafaxine during the study. They will be closely monitored for any changes in their depression symptoms. It's important to note that individuals with certain health conditions or those who have recently used specific medications may not qualify for the trial. Overall, this research aims to find faster and more effective treatment options for those suffering from severe depression, which can significantly impact their quality of life.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Current MDE in the context of unipolar major depressive disorder (DSM-5 criteria), hospitalized (open care) for this episode, with a minimum HDRS score of 24 and in the context of an indication for the introduction of venlafaxine treatment.
• • Patient aged between 18 and 65.
• • Signed free and informed consent
• • Membership of a social security scheme
• • For women of childbearing age, effective contraception throughout study participation.\* (\*Combined hormonal contraception (containing estrogen and progestin) associated with ovulation inhibition: (oral, intravaginal, transdermal), Progestin-only hormonal contraception associated with ovulation inhibition: (oral, injectable, implantable), Intrauterine device (IUD), Hormonal intrauterine system (IUS), Bilateral tubal occlusion, Vasectomized partner, Sexual abstinence.)
• Exclusion Criteria:
• • Criteria relating to associated pathologies entailing particular risks: pharmaco-resistant CDE (failure of at least two properly conducted treatments with two different antidepressant treatment classes), CDE with psychotic features, psychotic disorder, bipolar disorder, current (\<1 month) substance use disorder (excluding tobacco).
• • Liver impairment (AST and/or ALT \> 3 ULN, PAL and/or GGT and/or bilirubin \> 2 ULN).
• • Severe renal insufficiency (GFR \<30ml/min with Cockcroft's formula).
• • Bradycardia less than 55 beats per minute.
• • Contraindication to ketamine : Hypersensitivity to active substance or excipients, comatose state, central nervous system (CNS) depression, Parkinson's disease, Lewy body dementia, progressive supranuclear palsy, known prolongation of the QTc interval (\>450ms for men and \>470ms for women) or congenital long QT syndrome, recent acute myocardial infarction, uncompensated heart failure, history of ventricular arrhythmias or torsades de pointes, uncorrected hypokalemia (K+ \< 3. 5 mmol/l), epilepsy, uncontrolled hypertension, porphyria, history of stroke (CVA), intracranial hypertension.
• • Contraindication to venlafaxine (hypersensitivity to venlafaxine or excipients, are hereditary conditions of fructose intolerance, glucose-galactose malabsorption syndrome, or sucrase-isomaltase deficiency, unstable hypertension, no indication for venlafaxine treatment in clinician's opinion due to ineffectiveness or tolerability of previous venlafaxine treatment).
• • Current or previous treatment with venlafaxine or ketamine in the month prior to study inclusion.
• • Need to maintain another antidepressant, MAOI, Millepertuis or benzodiazepines (cyamemazine is permitted). Or potential drug interactions in case of recent cessation of these treatments (based on the Summary of Product Characteristics (SmPC) of the respective medication(s) and their half-life).
• • Any other unspecified reason (clinically significant illness or anomaly) which, in the opinion of the investigator or the sponsor, could compromise the safety of the participant.
• • Pregnant or breast-feeding patients (women of childbearing potential must have a negative urine or blood test for human chorionic gonadotropin prior to trial entry). Planned pregnancy within three months of enrolment
• • Adult under guardianship, curatorship or safeguard of justice
• • Participating in other interventional research involving the human body or within the exclusion period following previous research involving the human body, if applicable.
• • Social insurance
• Additional criteria for inclusion in the ancillary study :
• • - Contraindications to \[11C\]UCB-J PET-MRI
• • 1. Absolute contraindications: Pacemaker or neurosensorial stimulator or implantable defibrillator; clip on a brain aneurysm or vascular malformation; intraocular or intracerebral ferromagnetic foreign body; prostheses or objects or mobile ferromagnetic metal fragments; cochlear implants; peripheral stimulator; neurosurgical ventriculoperitoneal shunt valves; automated injection device such as insulin pump, glucose sensor; permanent eyelid or lip makeup; non-removable piercing; claustrophobia.
• • 2. Relative contraindications: Dental prostheses and orthodontic material; certain intrauterine devices; certain tattoos; certain transdermal patch implants; certain metal implants far from the examined area. (The investigator physician and/or radiology operator will always conduct a precise questionnaire before the examination to ensure perfect safety and absence of MRI danger)