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.
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
- 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
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.
- Conditions
- Treatment Resistant Depression
- 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:
- 0.5 mg/kg
- 0.6 mg/kg
- 0.75 mg/kg
- 0.9 mg/kg
- Further increments by 0.1-0.2 mg/kg, up to max 1.5 mg/kg
| Study group | Role | What they receive |
|---|---|---|
| Esketamine group | Active comparator | Dosing 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 ketamine | Active comparator | Treatment 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.
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)
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
Response - Montgomery-Asberg Depression Rating Scale (MADRS)
Response (≥50% improvement in MADRS)
Measured: Weeks 4, 8 and months 4 and 6
Remission - Montgomery-Asberg Depression Rating Scale (MADRS)
Remission (MADRS score ≤10)
Measured: Weeks 4, 8 and months 4 and 6
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.
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.
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.
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.
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.
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
Suicide attempts or gestures
Data collected as an Adverse Event of Special Interest
Measured: During 6-month study period
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.
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.
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.
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
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.
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.
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
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
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
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
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
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
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
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
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
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.
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.
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.
- First posted26 Feb 2024
- Study start3 Jun 2024
- Primary completionApr 2027 (estimated)
- Study completionApr 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Treatment Resistant DepressionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- The George Institute
- Sponsor type
- University, hospital or other
- Collaborators
- The University of New South Wales
- Responsible party
- Sponsor
- Investigators
- Colleen Loo, Principal investigator, The University of New South Wales
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
Study at a glance
From the registry record, last updated by the sponsor on 29 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparative Effectiveness Study of Two Forms of Ketamine for Treatment-Resistant Depression: a Randomised, Rater-blinded Trial
- ClinicalTrials.gov ID
- NCT06278779
- Acronym / sponsor ID
- TREK / X23-0311
- Conditions
- Treatment Resistant Depression
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 162 participants (estimated)
- Lead sponsor
- The George InstituteUniversity, hospital or other
- Collaborators
- The University of New South Wales
- Study start
- 3 Jun 2024 (actual)
- Primary completion
- Apr 2027 (estimated)
- Study completion
- Apr 2027 (estimated)
- First posted
- 26 Feb 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
- Model description
- Randomized, prospective, parallel group, comparative effectiveness trial.
| Arm | Type | Receives |
|---|---|---|
| Esketamine group | Active comparator | Drug: Esketamine groupDosing 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. |
| Racemic ketamine | Active comparator | Drug: Racemic ketamineTreatment 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. . |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (4 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Esketamine groupAlso: 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 | Drug | Esketamine group |
| Racemic ketamineTypically, 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 | Drug | Racemic ketamine |
Primary outcome
Montgomery-Asberg Depression Rating Scale (MADRS)
Time frame: From week 0 to week 4.
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.
28 secondary outcomes
Montgomery-Asberg Depression Rating Scale (MADRS) score
Time frame: At week 8, month 4 and month 6
Response - Montgomery-Asberg Depression Rating Scale (MADRS)
Time frame: Weeks 4, 8 and months 4 and 6
Remission - Montgomery-Asberg Depression Rating Scale (MADRS)
Time frame: Weeks 4, 8 and months 4 and 6
DASS-21
Time frame: Performed weekly from baseline to week 8 inclusive and at 6 month visit.
Clinical Global Impression-Improvement (CGI-I)
Time frame: Performed weekly from week 1 to week 4 inclusive, then at week 8 and at 3, 4, 5 & 6 month visits.
Clinical Global Impression-Severity (CGI-S)
Time frame: Performed weekly from baseline to week 4 inclusive, then at week 8 and at 3, 4, 5 & 6 month visits.
Columbia Suicide Severity Rating Scale (C-SSRS)
Time frame: Performed weekly from baseline to week 4 inclusive, then at week 8 and at 3, 4, 5 & 6 month visits.
Speed of response - Clinical Global Impression-Improvement (CGI-I)
Time frame: Performed weekly from week 1 to week 4 inclusive, then at week 8 and at 6 month visits.
Psychotomimetic symptoms
Time frame: Through study completion at each treatment visit, up to 6 months
Suicide attempts or gestures
Time frame: During 6-month study period
Number of Participants with urinary symptoms, as assessed using the Bladder Pain/ Interstitial Cystitis Symptom Score (BPIC-SS)
Time frame: Performed at baseline, week 4, week 8 and at 6 month visit.
Cognitive Failure Questionnaire scores (CFQ)
Time frame: Performed at baseline, week 4, week 8 and at 6 month visit.
Ketamine liking/craving score
Time frame: Performed at baseline, week 4, week 8 and at 6 month visit.
Number of Participants with urinary symptoms, as assessed using the Ketamine Side Effect Tool (KSET)
Time frame: Through study completion at each treatment visit, up to 6 months
Acceptability Questionnaire
Time frame: Performed at week 4, week 8 and at 6 month visit.
End of Treatment questionnaire
Time frame: Used at end of the treatment period(s) over the course of the study.
Recovering Quality of Life Questionnaire (REQOL-10)
Time frame: Over 6 month study period
WHO Disability Assessment Scale (WHODAS-12)
Time frame: Over 6 month study period
Patient Health Questionnaire-9 (PHQ-9)
Time frame: Over 6 month study period
Assessment of Quality of Life Questionnaire (AQoL-8D)
Time frame: Over 6 month study period
Resource Use Questionnaire (RUQ)
Time frame: Over 6 month study period
Treatment Preference
Time frame: Assessed once, prior to randomization
Stanford Expectations of Treatment Scale (SETS)
Time frame: Assessed once, after randomization and before first treatment
Difficulties in Emotion Regulation Scale-16 (DERS-16)
Time frame: Performed at baseline and week 4
Level of Personality Functioning Scale-Brief Form (LPFS-BF)
Time frame: Performed at baseline and week 4
Quick Inventory of Depressive Symptomatology Self-Report (QIDS-SR)
Time frame: Performed at baseline and the end of randomised treatment.
Patient Global Impression - Improvement (PGI-I)
Time frame: Performed weekly from week 1 to week 4 inclusive, then at week 8 and at month 3, 4, 5 & 6 visits.
Generalized Anxiety Disorder (GAD-7)
Time frame: Performed at baseline, week 4 and 8, and at month 3, 4, 5 and 6 visits.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 May 2026.
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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
Treatment Resistant Depression
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Colleen Loo principal investigator
The University of New South Wales
7 sites in 1 country: see every site and its status.
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.