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RecruitingNCT03320304RESTORE-LIFEUpdated Aug 27, 2026

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

An observational study in Treatment Resistant Depression, sponsored by LivaNova. Recruiting at 18 sites in 4 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-27.

Sponsored by LivaNova · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
500
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Treatment Resistant Depression

Keywords

  • Difficult to Treat Depression
  • TRD
  • VNS Therapy
  • Vagus Nerve Stimulation
  • VNS
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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).

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

Exclusion Criteria:

There are no exclusion criteria; the investigator should refer to the (local applicable) VNS Therapy Physician's Manual.

04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
500 participants (estimated)
Target follow-up
5 Years
Patient registry
Yes

Groups and cohorts

  • Vagal Nerve Simulation (VNS) Therapy

    The aim of this study is to include patients with difficult to treat depression from a global "real world" (standard of care) population who are referred for treatment with VNS Therapy.

    Device: Vagal Nerve Simulation (VNS) Therapy

Interventions

  • DeviceVagal Nerve Simulation (VNS) Therapy

    A VNS Therapy System used for vagus nerve stimulation and consisting of an implantable VNS Therapy generator, lead, and external programming system.

05

What researchers measure

Primary outcomes

  1. The primary endpoint of this study is response defined as reduction in Montgomery Åsberg Depression Rating Scale (MADRS) total score of at least 50% from baseline to 12 months post implant.

    MADRS is a 10-item diagnostic questionnaire used to measure the severity of depressive episodes in patients with mood disorders. Each item yields a score of 0 to 6. The overall score ranges from 0 to 60. Higher MADRS score indicates more severe depression. A 'Responder' is a subject that achieved ≥ 50% reduction from baseline in MADRS total score at the M12 assessment. A 'Non-Responder' is any patient who did not achieve ≥ 50% reduction from baseline in MADRS score at the M12 assessment. No formal hypothesis testing is presented; all the proposed statistical tests are descriptive in nature. The Primary endpoint analysis as defined above will be done only on patients that are enrolled while in a major depressive episode (MDE); the cut off point for current MDE at time of implant will be a MADRS score of 20. For the patients with a MADRS score below 20 at time of enrollment, only the continuous change in MADRS can be described (as the MADRS can only worsen or stay the same).

    Time frame: 12 months

Secondary outcomes

  1. Duration of response

    computed as the difference between the first recorded date post baseline that response is achieved (MADRS reduction from baseline ≥ 50%) and the first date at which MADRS again increased to a level of \<40% from baseline.

    Time frame: through study completion, an average of 4 years

  2. Change in MADRS

    Change in MADRS over time

    Time frame: through study completion, an average of 4 years

  3. Cumulative response

    Cumulative percentage of first-time MADRS responders (MADRS reduction from baseline ≥ 50%) at any post-baseline visit.

    Time frame: through study completion, an average of 4 years

  4. Cumulative remission

    Cumulative percentage of subjects in remission (MADRS ≤9) at any post-baseline visit.

    Time frame: through study completion, an average of 4 years

  5. Changes in depression score As measured by the Quick Inventory of Depressive Symptomatology Self-Report (QIDS-SR).

    The Quick Inventory of Depressive Symptomatology (QIDS-SR) is a 16-item, subject-completed questionnaire of the symptoms of mood and depression. The total score ranges from 0 to 27. A higher QIDS-SR score indicates a more severe depression.

    Time frame: through study completion, an average of 4 years

  6. Changes in mania score as measured by the Altman Self-Rating Mania Scale (ASRM)*.

    \*Optional assessments: to be done at selected sites only and based on investigator's clinical judgment to decide which subjects complete them. The Altman Self-rating Mania Scale (ASRM) is a 5-item self-reported diagnostic scale which can be used to assess the presence and severity manic and hypomanic symptoms, most commonly in patients diagnosed with bipolar disorder. The total score ranges from 0 to 20. A score of 6 or higher indicates a high probability of a manic or hypomanic condition.

    Time frame: through study completion, an average of 4 years

  7. Changes in Quality of Life as measured by the EuroQol five dimensions questionnaire (EQ-5D-5L)

    The EuroQol five dimensions questionnaire (EQ-5D-5L) is a standardized 5-item subject completed questionnaire measuring generic health status and quality of life.

    Time frame: through study completion, an average of 4 years

  8. Changes in patient function as measured by the Work Productivity and Activity Impairment Scale (WPAI)

    The Work Productivity and Activity Impairment Questionnaire (WPAI) is a subject self-reported 6-item questionnaire that measures impairments in work and activities. WPAI outcomes are expressed as impairment percentages, with higher numbers indicating greater impairment and less productivity.

    Time frame: through study completion, an average of 4 years

  9. Changes in Quality of Life and patient function as measured by the Quality of Life Enjoyment and Satisfaction Questionnaire - Short Form (Q-LES-Q-SF)

    The Quality of Life Enjoyment and Satisfaction Questionnaire - Short Form (Q-LES-Q-SF) is a standardized 16-item, self-report scale to assess the degree of enjoyment and satisfaction experienced by the subject during the past week.

    Time frame: through study completion, an average of 4 years

  10. Changes in suicidality as measured by item #10 of MADRS.

    Item 10 on the Montgomery-Åsberg Depression Rating Scale (MADRS) scale assesses suicidal thoughts as representing the feeling that life is not worth living, that a natural death would be welcome, suicidal thoughts and preparations for suicide and is rated from 0 to 6. A score of ≥ 4 ('probably better off dead') is of particular interest.

    Time frame: through study completion, an average of 4 years

  11. Changes in suicidality as measured by item #12 of QIDS-SR.

    For Item 12 of the Quick Inventory of Depressive Symptomatology (QIDS-SR), the subject assesses any thoughts of death or suicide over the previous 7 days on a 4- point scale; a score of ≥ 2 ('I think of suicide or death several times a week for several minutes') being of interest.

    Time frame: through study completion, an average of 4 years

  12. Changes in adjunctive antidepressant pharmacological treatment

    All adjunctive concomitant antidepressant and psychotropic medications will be collected

    Time frame: through study completion, an average of 4 years

  13. Changes in adjunctive antidepressant non-pharmacological treatment

    The following adjunctive non-pharmacological treatments will be collected: maintenance electroconvulsive therapy (ECT), Transcranial Magnetic Stimulation (TMS) and psychotherapy

    Time frame: through study completion, an average of 4 years

  14. Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]

    The following adverse events will be collected: serious adverse events, deaths, VNS Therapy related adverse events and device deficiencies.

    Time frame: through study completion, an average of 4 years

  15. Changes in cognition

    As measured by THINC-it® Tool\*. \*Optional assessments: to be done at selected sites only and based on investigator's clinical judgment to decide which subjects complete them.

    Time frame: through study completion, an average of 4 years

  16. Changes in anxiety as measured by the Generalized Anxiety Disorder Assessment (GAD 7)*.

    \*Optional assessments: to be done at selected sites only and based on investigator's clinical judgment to decide which subjects complete them. The Generalized Anxiety Disorder 7 (GAD-7) is a 7-item self-reported questionnaire for screening and severity measuring of generalized anxiety disorder (GAD). GAD-7 has seven items and uses a normative system of scoring. Assessment is indicated by the total score, which made up by adding together the scores for the scale all seven items.

    Time frame: through study completion, an average of 4 years

06

Study locations

11 of 18 sites recruiting
  • AKH Allgemeines Krankenhaus der Stadt Wien
    Vienna, 1090, Austria
    • Christoph Kraus, Dr. · Contact
    Recruiting
  • KU Leuven
    Leuven, Belgium
    • Koen Demyttenaere, Prof. · Contact
    Recruiting
  • Sozialstiftung Bamberg - Klinikum am Bruderwald
    Bamberg, Germany
    Withdrawn
  • Universitätsklinikum Bonn
    Bonn, Germany
    • Margaretha Klein, MD · Contact
    Recruiting
  • Universitätsklinikum Köln
    Cologne, Germany
    • Fritz-Georg Lehnhardt · Contact
    Recruiting
  • LVR-Hospital Essen
    Essen, 45147, Germany
    • Norbert Scherbaum, Prof. · Contact
    Recruiting
  • Universitätsklinikum Frankfurt
    Frankfurt, Germany
    • Christine Reif-Leonhard · Contact
    Recruiting
  • Universitätsklinikum Freiburg
    Freiburg im Breisgau, Germany
    Completed
  • Universitätsmedizin Göttingen
    Göttingen, Germany
    Withdrawn
  • Medizinische Hochschule Hannover
    Hanover, Germany
    Withdrawn
  • Universitätsklinikum Jena
    Jena, Germany
    Completed
  • Universitätsklinik Leipzig
    Leipzig, 04103, Germany
    • Maria Strauss, MD · Contact
    Recruiting
  • University Hospital Münster
    Münster, Germany
    • Bernhard Baune, Prof. · Contact
    Recruiting
  • Klinikum Wilhelmshaven
    Wilhelmshaven, Germany
    Active, not recruiting
  • Glenfield hospital
    Leicester, LE3 9EJ, United Kingdom
    • Ganesh Kunjithapatham, Dr. · Contact
    Recruiting
  • King's College London
    London, United Kingdom
    • Roland Zahn, Prof. · Contact
    Recruiting
  • Academic Psychiatry Wolfson Research Centre
    Newcastle upon Tyne, United Kingdom
    • Tiago da Silva Costa, Dr. · Contact
    Recruiting
  • Mendip HTT / St Andrew's Ward
    Wells, BA5 1TH, United Kingdom
    Active, not recruiting
07

References and documents

Publications

  • Kavakbasi E, Kraus C, Reif-Leonhard C, Blackwell JM, Dibue M, Treiber M, Achten S, Baune BT. Titration of vagus nerve stimulation for difficult-to-treat depression and onset of response: Early insights from the RESTORE-LIFE study. J Affect Disord. 2025 Jun 1;378:39-46. doi: 10.1016/j.jad.2025.02.047. Epub 2025 Feb 26. PubMed 40021060 ↗
  • Kavakbasi E, Baune BT. Combination of Acute and Maintenance Esketamine Treatment With Adjunctive Long-Term Vagus Nerve Stimulation in Difficult-to-Treat Depression. Neuromodulation. 2024 Jun;27(4):766-773. doi: 10.1016/j.neurom.2023.12.004. Epub 2024 Feb 10. PubMed 38340111 ↗
  • Kavakbasi E, Rosemann K, Yilmaz M, Vasileiadou A, Falcone V, Baune BT. Vagus Nerve Stimulation Combined With Alternating Synchronized and Nonsynchronized Intermittent Theta Burst Stimulation in Difficult-to-Treat Depression. J ECT. 2024 Mar 1;40(1):62-63. doi: 10.1097/YCT.0000000000000964. Epub 2023 Dec 28. No abstract available. PubMed 38194603 ↗
  • Young AH, Juruena MF, De Zwaef R, Demyttenaere K. Vagus nerve stimulation as adjunctive therapy in patients with difficult-to-treat depression (RESTORE-LIFE): study protocol design and rationale of a real-world post-market study. BMC Psychiatry. 2020 Sep 29;20(1):471. doi: 10.1186/s12888-020-02869-6. PubMed 32993573 ↗

Individual participant data

Plan to share: No

08

Registry details

Key details

Study ID
NCT03320304
Lead sponsor
LivaNova
Responsible party
Sponsor
First posted
Oct 25, 2017
Start date
Dec 14, 2017
Primary completion
Dec 1, 2029 (estimated)
Completion
Dec 1, 2031 (estimated)
Last update
Aug 27, 2026

Study contacts

Funda Basdar
Contact
funda.basdar@livanova.com
+32 473 97 49 41
Gaia Giannicola
Contact
Gaia.Giannicola@livanova.com
Koen Demyttenaere, Prof.
principal investigator · KU Leuven
Allan Young, Prof.
principal investigator · King's College

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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