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Treatment Resistant DepressionPhase 4TREKNCT06278779

Comparative Effectiveness Study of Two Forms of Ketamine for Treatment-resistant Depression

A Phase 4 study testing Esketamine group and Racemic ketamine in people with Treatment Resistant Depression, run by The George Institute at 7 sites in Australia.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this study is to compare the effectiveness of two formulations of ketamine - Spravato® and racemic ketamine - in people with treatment-resistant depression (TRD). The main questions it aims to answer are: How the two formulations compare in terms of their effectiveness in treating TRD. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Treatment Resistant Depression
What is being tested?
Esketamine group and Racemic ketamine
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
162 participants
Where
7 sitesAustralia
Study dates
3 Jun 2024to Apr 2027
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adult with treatment-resistant depression (TRD: not responded adequately to at least two different antidepressants of adequate dose and duration) who has a current depressive episode (DSM 5)
  • Assessed and attested by clinic psychiatrist as appropriate to receive either racemic ketamine or Spravato® ketamine treatment for TRD
  • MADRS score of ≥20 at study baseline, assessed by certified study rater
  • Aged ≥18 years
  • Written informed consent for research study obtained

Who cannot join

  • Not able to give informed consent
  • Any physical or mental condition which, in the opinion of the investigator, could interfere with study participation including outcome assessments
  • Any treatment with ketamine or Spravato® within 4 weeks prior to written informed consent for the research study
  • Patients who require an interpreter/translator for the clinic consent process, due to the infeasibility of obtaining an interpreter for research assessments, including self-rated scales

Trial locations and contacts

7 sites in 1 country. Contact the study team or a site near you to ask about taking part.

7 sites in 1 country

Australia7 sites, 7 recruiting
  • Royal Prince Alfred Hospital

    Camperdown, New South Wales, 2050

    Nicollette Thornton, SLHD-RPA-KetamineClinic@health.nsw.gov.au

    Nicholas Glozier

    Recruiting
  • Ramsay Clinic Albert Road

    Melbourne, Victoria, 3004

    Melanie Hurley, research.arc@ramsayhealth.com.au

    Malcolm Hopwood

    Recruiting
  • Royal Melbourne Hospital

    Parkville, Victoria, 3052

    Orli Schwartz, Study Coordinator, PHD, 61-3-8344-0944, orli@unimelb.edu.au

    Christopher Davey

    Recruiting
  • Black Dog Institute

    Randwick, New South Wales, 2031

    Angelo Alonzo, depressionclinic@blackdog.org.au

    Adam Bayes

    Recruiting
  • Gold Coast University Hospital

    Southport, Queensland, 4215

    Laura McCosker, +61 417207575, laura.mccosker2@health.qld.gov.au

    Shanthi Sarma

    Recruiting
  • Ramsay Clinic Northside

    St Leonards, New South Wales, 2065

    Yalda Pishyar, +61 2 8425 3022, neuroinfo.nsc@ramsayhealth.com.au

    Colleen Loo

    Recruiting
  • Ramsay Clinic Lakeside

    Warners Bay, New South Wales, 2282

    Hollie Ritchie, +61 3 4947 5169, ClinicalTrialsUnit.WBP@ramsayhealth.com.au

    Natasha Cairns, ClinicalTrialsUnit.WBP@ramsayhealth.com.au

    Recruiting

Other trials in Australia

About this study

Official title: Comparative Effectiveness Study of Two Forms of Ketamine for Treatment-Resistant Depression: a Randomised, Rater-blinded Trial

The goal of this study is to compare the effectiveness of two formulations of ketamine - Spravato® and racemic ketamine - in people with treatment-resistant depression (TRD). The main questions it aims to answer are:

  • How the two formulations compare in terms of their effectiveness in treating TRD.
  • How the two formulations compare in their acceptability to patients, safety, effects on patient quality of life and function, and cost effectiveness.

Participants will be randomised to receive either Spravato® or racemic ketamine treatment and asked to complete some questionnaires to assess the effects on mood, treatment acceptability, side effects, quality of life and function, and health economic outcomes.

Read the detailed description

The TREK study is a randomized, prospective, rater blinded (primary outcome raters), parallel group, comparative effectiveness trial of racemic ketamine and Spravato®, comparing their effectiveness, acceptability, safety, effects on quality of life (QOL), function and cost effectiveness after 4 weeks - 6 months of treatment in people with TRD.

Participants will be recruited from clinics/hospitals that are providing racemic ketamine and Spravato® treatment services for TRD. Participants will be referred, treated and followed up as per the clinic's normal clinical practice. Participants who consent to participate in this research study will undergo other processes in addition to the standard treatment procedures provided by their clinic:

  • Randomisation to receive racemic ketamine or Spravato®.
  • Completion of questionnaires to measure treatment effects on mood, acceptability, safety, quality of life and function and cost effectiveness.
Being tested
Esketamine group, Racemic ketamine
Medical subject headings
Depressive Disorder, Treatment-Resistant

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Esketamine groupDrug

    Also called Spravato®

    The recommended dosing for Spravato is:

    Weeks 1-4:

    Starting Day 1 dose:

    < 65 years: 56 mg

    ≥ 65 years: 28 mg

    Subsequent doses:

    28 mg (≥ 65 years), 56 mg or 84 mg twice weekly

    Weeks 5-8:

    28 mg (≥ 65 years), 56 mg or 84 mg once weekly

    From Week 9:

    28 mg (≥ 65 years), 56 mg or 84 mg every 2 weeks or once weekly

  • Racemic ketamineDrug

    Typically, dosing will begin at the standard dose of 0.5 mg/kg and adjusted as needed using an ascending dose titration schedule:

    1. 0.5 mg/kg
    2. 0.6 mg/kg
    3. 0.75 mg/kg
    4. 0.9 mg/kg
    5. Further increments by 0.1-0.2 mg/kg, up to max 1.5 mg/kg
Study groups in NCT06278779
Study groupRoleWhat they receive
Esketamine groupActive comparatorDosing of esketamine intranasal spray will be guided by the Spravato® Product Information. This involves a starting dosage of 28 or 56 mg, with dose adjustment up to 84 mg as required to optimise response. Dose adjustments will be based on effectiveness and tolerability to the previous dose. The recommended treatment protocol is twice per week for 4 weeks, then weekly in weeks 5-8, then option of weekly-fortnightly "maintenance" treatment for responders. After week 8, patients may continue treatment as guided by the ketamine clinic psychiatrist.
Receives: Drug: Esketamine group
Racemic ketamineActive comparatorTreatment administration will follow standard clinical practice in the recruiting clinic, with a recommendation to follow an evidence-based and established dose-optimising approach, given by injection, twice per week for 4 weeks, then the frequency of further treatments (week 5 - month 6) will be based on the clinical judgement of the ketamine clinic psychiatrist. Dosing will be adjusted by the ketamine clinic psychiatrist, based on clinical response, safety and tolerability. The psychiatrist will review the patient before each treatment, over the first 4 weeks, to judge the dose level required. Typically, dosing will begin at the standard dose of 0.5 mg/kg and adjusted using an ascending dose titration schedule if the patient has not shown clinical response and if side effects are adequately tolerated. .
Receives: Drug: Racemic ketamine

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Montgomery-Asberg Depression Rating Scale (MADRS)

    Change in score on the Montgomery-Asberg Depression Rating Scale (MADRS). The MADRS is sensitive to change, and is commonly used for treatment trials in depression.

    MADRS includes questions on ten symptoms, each of which yields a score of 0 to 6. The total score ranges from 0 to 60. The higher the MADRS score the more severe the depression. Cutoff points are for levels of depression are:

    0 to 6: normal /symptom absent 7 to 19: mild depression 20 to 34: moderate depression 35 to 60: severe depression.

    Measured: From week 0 to week 4.

Secondary outcomes (28)
  1. Montgomery-Asberg Depression Rating Scale (MADRS) score

    Score on the Montgomery-Asberg Depression Rating Scale (MADRS). The MADRS is sensitive to change, and is commonly used for treatment trials in depression. See outcome 1 for minimum and maximum values, and whether higher scores indicate a better or worse outcome.

    Measured: At week 8, month 4 and month 6

  2. Response - Montgomery-Asberg Depression Rating Scale (MADRS)

    Response (≥50% improvement in MADRS)

    Measured: Weeks 4, 8 and months 4 and 6

  3. Remission - Montgomery-Asberg Depression Rating Scale (MADRS)

    Remission (MADRS score ≤10)

    Measured: Weeks 4, 8 and months 4 and 6

  4. DASS-21

    Depression, Anxiety and Stress Scale (DASS-21) - will be used to measure psychological distress. It consists of three 7-item subscales, with items scored on a 4-point Likert scale (0-3) and summed to obtain subscale scores.

    Measured: Performed weekly from baseline to week 8 inclusive and at 6 month visit.

  5. Clinical Global Impression-Improvement (CGI-I)

    The Clinical Global Impression - Improvement scale (CGI-I) is used to assess depressive symptom improvement from study baseline. The minimum value is -6 (maximum deterioration) and the maximum value is 6 (ideal improvement).

    Measured: Performed weekly from week 1 to week 4 inclusive, then at week 8 and at 3, 4, 5 & 6 month visits.

  6. Clinical Global Impression-Severity (CGI-S)

    The Clinical Global Impression - Severity scale (CGI-S) is used to assess depressive symptom severity. The minimum value is 1 (normal) and the maximum value is 7 (among the most extremely ill patients).

    Measured: Performed weekly from baseline to week 4 inclusive, then at week 8 and at 3, 4, 5 & 6 month visits.

  7. Columbia Suicide Severity Rating Scale (C-SSRS)

    Columbia Suicide Severity Rating Scale (C-SSRS) - short questionnaire that will be used by the clinic teams as a clinical tool to assess suicidality.

    Measured: Performed weekly from baseline to week 4 inclusive, then at week 8 and at 3, 4, 5 & 6 month visits.

  8. Speed of response - Clinical Global Impression-Improvement (CGI-I)

    Speed of response, assessed by number of treatments required to attain CGI-I score of ≥ 3.

    Measured: Performed weekly from week 1 to week 4 inclusive, then at week 8 and at 6 month visits.

  9. Psychotomimetic symptoms

    Assessed via the Ketamine Side Effect Tool (KSET), designed to monitor the acute, cumulative and longer-term safety of ketamine treatment.

    Measured: Through study completion at each treatment visit, up to 6 months

  10. Suicide attempts or gestures

    Data collected as an Adverse Event of Special Interest

    Measured: During 6-month study period

  11. Number of Participants with urinary symptoms, as assessed using the Bladder Pain/ Interstitial Cystitis Symptom Score (BPIC-SS)

    Bladder Pain-Interstitial Cystitis Symptom Score (BPIC-SS) - a self-report symptom-based instrument that identifies moderate to severe bladder pain syndrome. Side effects of racemic ketamine/Spravato® include inflammation of the bladder endothelium. From 8 questions about bladder/urination pain, patients can score a minimum of 0 (asymptomatic) and a maximum of 38 (severe symptoms).

    Measured: Performed at baseline, week 4, week 8 and at 6 month visit.

  12. Cognitive Failure Questionnaire scores (CFQ)

    Cognitive Failures Questionnaire (CFQ) is a self-rated tool to assess subjective impression of cognitive functioning. From 25 questions, patients can score a minimum of 0 (best) and a maximum of 100 (worst).

    Measured: Performed at baseline, week 4, week 8 and at 6 month visit.

  13. Ketamine liking/craving score

    Ketamine liking/craving score will be used as a measure of ketamine craving/abuse. A visual analogue scale is used, where patients can score a minimum of 0 (strong dislike/no craving) and a maximum of 30 (very strong liking/constant craving).

    Measured: Performed at baseline, week 4, week 8 and at 6 month visit.

  14. Number of Participants with urinary symptoms, as assessed using the Ketamine Side Effect Tool (KSET)

    Assessed via the Ketamine Side Effect Tool (KSET), designed to monitor the acute, cumulative and longer-term safety of ketamine treatment.

    Measured: Through study completion at each treatment visit, up to 6 months

  15. Acceptability Questionnaire

    An 8-item self-rated instrument to assess the acceptability of healthcare interventions. This evaluates the constructs of affective attitude, effort burden, ethicality, perceived effectiveness, intervention coherence, self-efficacy, opportunity costs and general acceptability. Patients can score a minimum of 8 (very unacceptable) and a maximum of 40(very acceptable).

    "If reporting a score on a scale, please include the minimum and maximum values, and whether higher scores mean a better or worse outcome." Appears that not all high scores are positive so makes it hard to address this issue.

    Measured: Performed at week 4, week 8 and at 6 month visit.

  16. End of Treatment questionnaire

    Collected via case report form. Captures reason for ceasing, switching or re-starting study medication.

    Measured: Used at end of the treatment period(s) over the course of the study.

  17. Recovering Quality of Life Questionnaire (REQOL-10)

    Recovering Quality of Life, 10-item (REQOL-10) is used to assess the quality of life for people with different mental health conditions. Patients can score a minimum of 0 (poorest quality of life) and a maximum of 40 (highest quality of life).

    Measured: Over 6 month study period

  18. WHO Disability Assessment Scale (WHODAS-12)

    12-item WHO Disability Assessment Scale (WHODAS-12) is a 12-item self-rated assessment of health and disability. It will be used to assess functionality. Patients can score a minimum of 0 (no disability) and a maximum of 48 (complete disability).

    Measured: Over 6 month study period

  19. Patient Health Questionnaire-9 (PHQ-9)

    Patient Health Questionnaire-9 (PHQ-9) is a self-report screening tool designed to assess the severity of depressive symptoms in individuals and monitors symptom changes and treatment effects over time. Patients can score a minimum of 0 (no depression) and a maximum of 27 (severe depression).

    Measured: Over 6 month study period

  20. Assessment of Quality of Life Questionnaire (AQoL-8D)

    Assessment of Quality of Life Questionnaire (AQoL-8D) consists of 35 items covering 8 dimensions: Independent Living, Pain, Senses, Mental Health, Happiness, Coping, Relationships, and Self-worth. It will be used to assess quality of life outcomes and to facilitate the health economics analysis. There is a max patient score of 1 (perfect health) and a minimum score of 0 (deceased) based on weighted utility scores

    Measured: Over 6 month study period

  21. Resource Use Questionnaire (RUQ)

    The resource use questionnaire (RUQ) collects information regarding the type and number of contacts with the health system including hospitalisations, consultations and medications. The information is then 'scored' by multiplying indicative unit costs by the number of contacts for each service used. The costs per service are summed to calculate a total health sector cost.

    The resource use questionnaire also collects information regarding time missed (absenteeism) and time working at reduced capacity (presenteeism) for paid work and time missed from unpaid work. The number of hours missed and working at reduced capacity from paid work will be valued using an average wage rate. The hours missed from unpaid work will be valued using a shadow cost for the value of leisure time. These costs are summed and combined with health sector costs to calculate societal costs.

    Measured: Over 6 month study period

  22. Treatment Preference

    The Treatment Preferences questionnaire is a simple 3 item self-report questionnaire which asks participants to indicate their treatment preference for one of the 2 interventions, if any; their strength of preference (slight, moderate or strong); their reason for preference (Prefer this method of receiving the medication; Had this treatment before and benefitted; Past negative experience with the other treatment; Impression from reports, other people or media; Other (please specify))

    Measured: Assessed once, prior to randomization

  23. Stanford Expectations of Treatment Scale (SETS)

    The SETS is a self-report questionnaire that assesses positive and negative treatment expectations with 6 items rated on a 7-point Likert scale from 0 'not agree at all' to 6 'fully agree'; additional questions ask the responder to confirm the treatment they will receive and whether they have received it before as well as whether any specific benefits or harms/negative side effects are expected

    Measured: Assessed once, after randomization and before first treatment

  24. Difficulties in Emotion Regulation Scale-16 (DERS-16)

    The DERS-16 is a self-report measure with established internal consistency, reliability and validity that assesses an individual's typical levels of difficulties in emotion regulation. The DERS-16 assesses five aspects of difficulties in emotion regulation: nonacceptance of emotional responses, difficulty engaging in goal-directed behaviour, impulse control difficulties, limited access to emotion regulation strategies, and lack of emotional clarity.

    Measured: Performed at baseline and week 4

  25. Level of Personality Functioning Scale-Brief Form (LPFS-BF)

    The LPFS-BF is a 12-item self-report questionnaire that provides a first impression of impairments in personality functioning. The LPFS-BF consists of 12 items, clustered into two higher order domains: self-functioning and interpersonal functioning. Validity and sensitivity have been established in a range of samples and languages

    Measured: Performed at baseline and week 4

  26. Quick Inventory of Depressive Symptomatology Self-Report (QIDS-SR)

    The Quick Inventory of Depressive Symptomatology self-report (QIDS-SR) is a measure of depressive symptom severity. It consists of 16 factors across 9 different criterion domains, with items scored on a 4-point Likert scale (0-3) and summed to obtain subdomain scores.

    Measured: Performed at baseline and the end of randomised treatment.

  27. Patient Global Impression - Improvement (PGI-I)

    The Patient Global Impression - Improvement (PGI-I) measures a patient's perception of their improvement since a treatment. It consists of one question that uses a 7-point scale that asks a patient to rate their change ranging from 'very much improved' to 'very much worse'.

    Measured: Performed weekly from week 1 to week 4 inclusive, then at week 8 and at month 3, 4, 5 & 6 visits.

  28. Generalized Anxiety Disorder (GAD-7)

    The Generalized Anxiety Disorder (GAD-7) is used to assess symptom severity of generalised anxiety disorder. It consists of 7 items that use a 4-point Likert scale (0-3) which are summed to create a total score ranging from 0 (minimal anxiety) to 21 (severe anxiety.

    Measured: Performed at baseline, week 4 and 8, and at month 3, 4, 5 and 6 visits.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Feb 2024
  2. Study start3 Jun 2024
  3. Primary completionApr 2027 (estimated)
  4. Study completionApr 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized, prospective, parallel group, comparative effectiveness trial.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
162 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06278779
Sponsor's protocol ID
X23-0311
Acronym
TREK
Status last verified
May 2025
First submitted
20 Jan 2024
Last updated
29 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Esketamine group and Racemic ketamine in people with Treatment Resistant Depression, run by The George Institute at 7 sites in Australia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 29 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 7 sites in Australia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Abigail Hansen (80524300, Trek@georgeinstitute.org.au), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Montgomery-Asberg Depression Rating Scale (MADRS) (time frame: From week 0 to week 4.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 May 2026.

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