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.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
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
Where Is This Study? (4 UK sites)
Glenfield hospital
Leicester LE3 9EJ, United Kingdom
King's College London
London, United Kingdom
Academic Psychiatry Wolfson Research Centre
Newcastle upon Tyne, United Kingdom
Mendip HTT / St Andrew's Ward
Wells BA5 1TH, United Kingdom
How to Get in Touch
Funda Basdar
Sponsor contactCONTACT
Gaia Giannicola
Sponsor contactCONTACT
