Depression and Anxiety Trial, Recruiting NCT06396312 Sponsor: Max-Planck-Institute of Psychiatry Condition: Depression and Anxiety
Back to Depression And Anxiety

Depression and Anxiety Trial, Recruiting

NCT06396312
Recruiting Not Applicable

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who may be able to join

  • People who have agreed to participate in the "Biobanking" program at the Max Planck Institute of Psychiatry
  • People aged 18 or older
  • People who have been formally diagnosed with Major Depressive Disorder (a serious type of depression) confirmed by a structured interview
  • People whose depression has not responded to at least one or two previous treatments (known as treatment-resistant depression, stage I or II)
  • People for whom antidepressant medication has been recommended by their doctor
  • People for whom a doctor has recommended adding lithium (a mood-stabilising medication) to their treatment
  • People who are able to understand the study and give their written agreement to take part

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • People under the age of 18
  • People with certain health conditions that make taking lithium unsafe (confirm with trial site)
  • People who have previously experienced a hypomanic or manic episode (periods of unusually high or elevated mood and energy)
  • People taking two or more antidepressant medications at the same time as lithium, unless one of those medications is specifically used to help with sleep, such as Mirtazapine, Mianserin, or Trazodone
  • People already using a different add-on medication strategy alongside lithium
  • People taking more than 100 mg in total of Quetiapine (a psychiatric medication), in either its immediate- or extended-release form
  • People currently experiencing a substance use disorder, except for moderate alcohol or benzodiazepine use related to the current episode of depression, or smoking
  • People considered unsuitable for the study by the investigator for any reason
  • People with significant conditions affecting the brain or nervous system, such as stroke, brain tumours, epilepsy (current or past), brain inflammation or autoimmune conditions affecting the brain, traumatic brain injury, or prior brain surgery
  • People who are not able to give informed consent
  • People who have received electroconvulsive therapy (ECT) during their current episode of depression
  • People who have received repetitive transcranial magnetic stimulation (rTMS) during their current episode of depression

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 30 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Peter Falkai, MD, Max-Planck-Institute of Psychiatry

Phone: 0049-89-30622-1418

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Max-Planck-Institute of Psychiatry
Registry
ClinicalTrials.gov
Start date
2 April 2024
Est. completion
1 April 2028

Where this trial is recruiting

🇩🇪 Germany

Primary endpoints

multimodal and multivariate signature to predict outcome of lithium augmentation

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 30 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov