Depression and Anxiety Trial, By Invitation NCT06044324 Sponsor: First Affiliated Hospital of Zhejiang University Condition: Depression and Anxiety
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Depression and Anxiety Trial, By Invitation

NCT06044324
By Invitation 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 tried two or more antidepressant medications (working in different ways) that did not work well enough, and who have been on a stable dose of an antidepressant for more than 6 weeks before joining — with "not working well enough" defined as less than a 50% improvement on a standard depression rating scale (HAMD-24).
  • People who score 20 or higher on the 24-item Hamilton Depression Scale (HAMD-24), which is a standard tool used to measure how severe depression is.
  • People with normal vision, or vision that is fully corrected (for example, with glasses or contact lenses).
  • People who are able to complete a specific visual perception test used in this study (confirm with trial site for details).
  • People who have completed at least a college-level education.
  • People aged 18 to 45 years, of any gender.
  • People who are right-handed.
  • People of Han Chinese ethnicity.
  • People who have read and signed a written consent form and are willing to take part in the study and its assessments.

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 who have another mental health condition alongside depression, such as schizophrenia, intellectual disability, or substance dependence.
  • People who have metal objects inside their body, or any other reason that makes a PET-MRI scan unsafe for them.
  • People who have a serious or unstable physical health condition.
  • Women who are pregnant or breastfeeding, or women of childbearing age whose urine pregnancy test comes back positive during the screening period.
  • People who take benzodiazepine medications (a type of sedative or anti-anxiety medicine) during the study period.
  • People whom the study investigators feel, for any other reason, should not take part in this trial.

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 23 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.

GP referral letter

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Trial details

Status
By Invitation
Phase
Not Applicable
Sponsor
First Affiliated Hospital of Zhejiang University
Registry
ClinicalTrials.gov
Start date
1 November 2023
Est. completion
1 December 2025

This date has passed while the registry still lists the trial as open to participants. Sponsors often update a trial's status without revising its projected end date, so it may well still be recruiting — but the record is out of date in at least one respect. Check with the study contact before relying on either.

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Change in Suppression Index after treatment; Change in Suppression Index after treatment; Hamilton Depression Scale (24-items) Total Score Change; Hamilton Depression Scale (24-items) Total Score Change; Change in synaptic density using positron emission tomography/magnetic resonance imaging; Change in synaptic density using positron emission tomography/magnetic resonance imaging

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: 23 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