Treatment Resistant Depression and Vagus Nerve Stimulation
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| 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 |
More Assistance Publique - Hôpitaux de Paris trials in France
Other trials for the same condition
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