A Prospective Multi-center Randomized Controlled Blinded Trial Demonstrating the Safety and Effectiveness of VNS Therapy System as Adjunctive Therapy Versus a No Stimulation Control in Subjects With Treatment-Resistant Depression

  • End date
    Dec 31, 2030
  • participants needed
  • sponsor
Updated on 23 September 2021
Tina Marzullo
Primary Contact
AMR- Baber Research, Inc. (2.9 mi away) Contact
+71 other location
depressive disorder
depressive symptoms
depressive episode


Objectives of this study are to determine whether active VNS Therapy treatment is superior to a no stimulation control in producing a reduction in baseline depressive symptom severity, based on multiple depression scale assessment tools at 12 months from randomization.


A prospective, multi-center, randomized, controlled, blinded trial of subjects implanted with VNS Therapy. Active treatment and no stimulation control are randomized, at least two weeks after implantation and observed for 12-months.

After completing the 12 month endpoint in the RCT portion of the study, all RECOVER subjects will transition into the prospective, open-label, longitudinal portion of the study. Subjects in the control arm of RECOVER will be activated after completing the 12 month endpoint.

After completion of enrollment in the RCT portion or meeting of interim success criterion (whichever comes first), up to 5,800 new subjects may enroll directly into the open-label,prospective, longitudinal study. These subjects will participate in the study for approximately 5 years.

The study has been designed in accordance with The Centers for Medicare and Medicaid Services coverage with evidence development (CED) decision entitled "Decision Memo for Vagus Nerve Stimulation (VNS) for Treatment Resistant Depression (TRD) (CAG-00313R2).

Condition Treatment Resistant Depression
Treatment Vagus Nerve Stimulation (VNS)
Clinical Study IdentifierNCT03887715
Last Modified on23 September 2021


Yes No Not Sure

Inclusion Criteria

The patient must be in a major depressive disorder (MDD) episode for two years
or have had at least four episodes of MDD, including the current episode
The patient's depressive illness meets a minimum criterion of four prior
failed treatments of adequate dose and duration as measured by a tool designed
for this purpose
The patient is experiencing a major depressive episode (MDE) as measured by a
guideline recommended depression scale assessment tool on two visits, within a
-day span prior to implantation of the VNS device
Patients must maintain a stable medication regimen for at least four weeks
before device implantation

Exclusion Criteria

Current or lifetime history of psychotic features in any MDE
Current or lifetime history of schizophrenia or schizoaffective disorder
Current or lifetime history of any other psychotic disorder
Current or lifetime history of rapid cycling bipolar disorder
Current secondary diagnosis of delirium, dementia, amnesia, or other cognitive
Current suicidal intent; or
Treatment with another investigational device or investigational drugs
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