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A Study to Assess Effectiveness and Efficiency of VNS Therapy in Patients With Difficult to Treat Depression.

Sponsor: LivaNova

NCT ID: NCT03320304

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Vagal Nerve Simulation (VNS) Therapy (device)
How long the study runs
Study runs about 168 months (dates as stated)
About the drug or intervention
Vagal Nerve Simulation (VNS) Therapy — device: A VNS Therapy System used for vagus nerve stimulation and consisting of an implantable VNS Therapy generator, lead, and external programming system.
Patient visit burden
Not specified by the sponsor

In plain English

This study looks at how well VNS Therapy (vagus nerve stimulation) works for people whose depression has not improved after trying several antidepressant treatments. This is sometimes called treatment resistant depression. People who take part keep their current treatment, and the study is funded by LivaNova.

Who can take part

  • You are aged 18 or over.
  • You have depression that has lasted more than 2 years, or you have had 2 or more separate episodes of depression.
  • Your depression has not got better enough after trying an adequate number of antidepressant treatments. A short interview called the MINI (Mini International Neuropsychiatric Interview) is used to confirm your diagnosis.
  • You are already having at least one treatment, such as antidepressant medicine, maintenance electroconvulsive therapy (ECT), or talking therapy. If you have bipolar disorder, this could be a mood-stabilising medicine such as lithium, an anticonvulsant, or an antipsychotic.
  • You are able and willing to attend outpatient clinic visits and complete all the study checks.
  • You give written permission (informed consent) to take part.

Who may not be able to

  • Severe learning disability.
  • Current severe or significant alcohol or drug misuse.
  • A diagnosis of schizophrenia or another psychosis-related condition.
  • Borderline or severe personality disorder, if the study doctor believes it would significantly interfere with taking part.
  • No other reasons for exclusion are listed — the study team will refer to the VNS Therapy Physician's Manual, so ask the trial team if unsure.

What taking part involves

  • • VNS Therapy (vagus nerve stimulation) for difficult-to-treat depression — how it is given is not stated — ask the trial team.
  • • You continue with your current antidepressant or mood-stabilising treatment during the study.
  • • Regular outpatient clinic visits and completing all the study checks.

Time commitment: Taking part involves regular outpatient clinic visits and completing all study evaluations; how often the visits are and how long the study lasts are not stated — ask the trial team.

Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.

Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
500
Started
2017-12-14
Last checked
2026-08

Plain English Summary

What is this study?

  • • Testing a new treatment for treatment resistant depression
  • • Clinical study - 500 participants
  • • The primary objective of this study is to assess short, mid and long-term clinical outcomes in patients with difficult to treat depression (such as patients with treatment resistant depression) treated with Vagus Nerve Stimulation (VNS) Therapy as adjunctive therapy

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with treatment resistant depression

Where?

  • • Leicester - Glenfield hospital
  • • London - King's College London
  • • Newcastle upon Tyne - Academic Psychiatry Wolfson Research Centre
  • • Wells - Mendip HTT / St Andrew's Ward

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The primary objective of this study is to assess short, mid and long-term clinical outcomes in patients with difficult to treat depression (such as patients with treatment resistant depression) treated with Vagus Nerve Stimulation (VNS) Therapy as adjunctive therapy.

More detail

The population under study comprises a real-world patient population with difficult to treat depression: patients diagnosed with unipolar or bipolar disorder with chronic or recurrent depression who fail to achieve an adequate response to standard psychiatric management. The diagnosis of depression and comorbid disorders will be determined based on the Mini International Neuropsychiatric Interview (MINI). A minimum of five hundred (500) patients will be implanted with a VNS Therapy System and up to eighty (80) sites may participate in this study. Enrollment will take 11 years, based on competitive enrollment. For each subject a baseline visit will occur between 1 and 6 weeks before implant. Once implanted with the device, subjects will be followed-up for a minimum of 36 months and a maximum of 60 months. The study may stop when the last subject has reached the 36 months follow-up.

Treatment Resistant Depression

How this trial compares with your answers

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Be at least 18 years of age.

Who cannot take part

  • ✗There are no exclusion criteria; the investigator should refer to the (local applicable) VNS Therapy Physician's Manual.
See the full criteria
Inclusion Criteria: * Be at least 18 years of age. * Have a documented primary diagnosis of chronic (\>2 years) or recurrent (2 or more prior episodes) major depressive episode that has not adequately responded to an adequate number of antidepressant treatments, as per local medical standards. This diagnosis must be confirmed using the MINI. * Provide written Ethics Committee (EC) or Institutional Review Board (IRB) approved informed consent and Health Insurance Portability and Accountability Act (HIPAA, US only) authorization (as applicable according to local requirements). * Currently is receiving at least one antidepressant treatment (i.e., antidepressant drug, maintenance electroconvulsive therapy, or formal psychotherapy including supportive psychotherapy) or mood stabilizing treatment for bipolar patients (such as lithium, anticonvulsants, or atypical antipsychotics). * Able and willing to comply with the frequency of (outpatient) clinic visits and to reliably complete all the evaluations as specified in the study protocol.Hence based on the nature of their disease, the following patients should not be included: patients with mental retardation, current severe or significant substance/alcohol abuse, diagnosis of one or more schizophrenia-spectrum or other psychotic disorders, diagnosis of borderline or severe personality disorder as determined by clinical judgment which, in the investigator's opinion, would significantly interfere with subject's participation in the study) Exclusion Criteria: There are no exclusion criteria; the investigator should refer to the (local applicable) VNS Therapy Physician's Manual.

Where Is This Study? (4 UK sites)

Glenfield hospital

Leicester LE3 9EJ, United Kingdom

Recruiting

King's College London

London, United Kingdom

Recruiting
Hospital R&D contact (matched)

Jasmine Palmer

kch-tr.research@nhs.net0203 299 1980

Academic Psychiatry Wolfson Research Centre

Newcastle upon Tyne, United Kingdom

Recruiting

Mendip HTT / St Andrew's Ward

Wells BA5 1TH, United Kingdom

ACTIVE_NOT_RECRUITING

How to Get in Touch

Funda Basdar

Sponsor contact

CONTACT

+32 473 97 49 41 funda.basdar@livanova.com

Gaia Giannicola

Sponsor contact

CONTACT

Gaia.Giannicola@livanova.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-08