Ireland
--:--IST
Recruiting Not applicable

Treatment Resistant Depression and Vagus Nerve Stimulation

NCT05952674 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-02-19
Last updated
2026-06-23

Condition(s) studied

Treatment Resistant Depression (TRD)

Investigational drug(s) / intervention(s)

Vagus Nerve Stimulation (VNS)Best Medical Treatment

Vagus Nerve Stimulation (VNS): The surgical intervention for the implantation of the VNS medical device is performed by a neurosurgeon under general anesthesia and lasts about an hour. Two incisions are made on the left: one incision to implant an electrode wrapped around the vagus nerve, the other incision to implant the stimulator. The electrode and the stimulator are connected by a cable tunneled. The cardiac tolerance is usually tested at the end of the surgery by turning on the neurostimulator for a few minutes. The stimulator is turned on about two weeks after the implantation, and after the neurosurgeon has checked the quality of healing. The settings used in first intention are standardized and derived from the parameters usually used for the treatment of epilepsies: a pulse width of 250μs, a stimulation frequency of 30Hz, and a 30sec stimulation cycle (ON) every 5min (OFF). Intensity is progressively increased by steps of 0.25mA to reach the 1.5-2mA range, depending on stimulation-induced side effects.

Best Medical Treatment: Best Medical Treatment for resistant depression.

Study summary

Depression is a common illness, affecting 17% of the population over the course of a lifetime. A third of depressions relapses and progresses to recurrence and resistance to treatments. Despite the optimization of antidepressant medical strategies, 20 to 40% of depressions do not respond to treatment. This is particularly worrying as 6% of non-responder patients will die by committing suicide.

Depression has a major impact on quality of life, socio-professional functioning and healthcare consumption.

Sometimes, TRD is part of a bipolar illness. In this case, the challenge is even bigger because antidepressants are no well tolerated, further reducing the therapeutic options in case of resistance, the severity and duration of the depressive episodes are the main factors explaining the deterioration of the quality of life and the increasing cost of cares for these patients.

The standard treatment for TRD is electroconvulsive therapy (ECT), which results in a response in 60 to 70% of cases after a few weeks of treatment. However, the improvement is often transient and 40% of patients relapse within 6 months of the initial ECT session. Moreover, ECT is often not well tolerated. This therapeutic impasse therefore makes TRD a priority public health target to which it is urgent to provide a realistic medico-economical response.

The literature suggests that Vagus Nerve Stimulation (VNS) has unique kinetics of efficacy in depression, particularly in preventing long-term recurrences, and therefore responding to the lack of effective maintenance treatment in TRD. In fact, the benefits of VNS gradually accumulate over 12-24 months, which makes it complementary to more incisive treatments like ECT. Finally, its efficacy-tolerance profile appears to be similar in uni and bipolar TRD, giving VNS a potentially unique place in the therapeutic arsenal in psychiatry.

The DepVNS hypothesis is that VNS is a medico-economically efficient therapeutic option to overcome the therapeutic impasse in which patients suffering from uni and bipolar DR currently find themselves due to the frequency of relapses under treatment.

The primary objective is to estimate, from a collective point of view, the incremental cost-utility ratio of VNS to treat patients suffering from RD.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18 years and older ; * Childbearing women must have an efficient contraception for the whole study period * Diagnosis of recurrent depressive trouble or persistent depressive disorder or bipolar disorder (according to DSM-5) * Start of disorder (defined by the occurrence of the first thymus episode: characterized depressive disorder or maniac episode with or without mixed characteristics) for 5 years or more * At least one of the following criteria: * Criterion A: current characterized depressive disorder and characterized depressive disorder for at least 12 months during the last 24 months despite at least four treatments lines at appropriate dosage and duration * Criterion B: current treatment by ECT/(Es)Ketamine/TMS and criteria A before the start treatment or ECT/(Es)Ketamine/TMS dependency * Patients who, after the nature of the study has been explained to them, have given written consent Exclusion Criteria: * Know pregnancy or breastfeeding * Schizophrenia, schizoaffective disorder or persistent delusional disorder (DSM-5) * Characterized depressive disorder with psychotic characteristics within 3 months before the inclusion (DSM-5) * Concomitant participation to another interventional research not authorized by the coordinating investigator or the scientific lead. Participation to non-interventional researches is allowed. * Patients receiving enforced cares (ASPDT, ASPPI, ASPDRE, etc.) * Non-affiliation to a social security regimen or any other social protection regimen * Disability, according to the investigator, to understand the study or refusal to sign the study consent form (non-francophone patient, cognitive disorders) * Anticipated disability to attend all the visits, treatments and measures planned by the protocol: severe personality disorder, severe substance addiction, severe intellectual development disorder. In any of those cases, the notion of severity is at the indiscretion of the investigator Secondary Exclusion Criteria: * Surgical contraindication to the VNS * Positive β-HCG (results obtained after the informed consent is signed but before the randomization)

Primary outcome measure(s)

  • Cost-utility of VNS — Month 24
    Incremental cost-utility ratio of the Vagus Nerve Stimulation (group VNS + optimal medical treatment) in comparison to the control group (optimal medical treatment only) within 24 months of VNS placement

Trial sites (24)

FacilityCityRegionStatus
CHU Angers Angers France Active Not Recruiting
Centre Hospitalier Charles Perrens Bordeaux France Recruiting
CHU Caen Caen France Not Yet Recruiting
CHU Clermont-Ferrand, Hôpital Gabriel Montpied Clermont-Ferrand France Recruiting
AP-HP. Nord - Université de Paris, Hôpital Louis Mourier Colombes France Withdrawn
APHP. Hôpitaux Universitaires Henri Mondor, Hôpital Henri Mondor Créteil France Recruiting
CHU Dijon, Hôpital Le Bocage Dijon France Recruiting
CHU Grenoble Alpes Grenoble France Recruiting
AP-HP. Université Paris Saclay, Hôpital Bicêtre Le Kremlin-Bicêtre France Withdrawn
CHU Lille Lille France Recruiting
Hospices Civils de Lyon, Hôpital Pierre Wertheimer Lyon France Not Yet Recruiting
Assistance Publique Hôpitaux de Marseille, Hôpital de la Conception Marseille France Not Yet Recruiting
CHU de Nantes, Hôtel Dieu Nantes France Recruiting
CHU Nice, Hôpital Pasteur 1 Nice France Recruiting
AP-HP. Sorbonne Université, Hôpital La Pitié Salpetrière Paris France Active Not Recruiting
GHU Paris Psychiatrie & Neuroscience, site Saint Anne Paris France Recruiting
Centre Hospitalier Henri Laborit Poitiers France Not Yet Recruiting
Centre Hospitalier Guillaume Regnier Rennes France Recruiting
CHU Rouen, Centre Hospitalier du Rouvray Rouen France Recruiting
CHU Saint-Etienne Saint-Etienne France Recruiting
CHU Toulouse, Hôpital de Psychiatrie Toulouse France Recruiting
CHRU Tours, Clinique Psychiatrique Universitaire Tours France Recruiting
CHU Brest Brest France Not Yet Recruiting
AP-HP. Centre - Université de Paris, Hôpital Corentin-Celton Issy-les-Moulineaux France Withdrawn
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05952674 on ClinicalTrials.gov ↗ ← All trials in France