Depression and Anxiety Trial, Recruiting NCT05661383 Sponsor: Hôpital le Vinatier Condition: Depression and Anxiety
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Depression and Anxiety Trial, Recruiting

NCT05661383
Recruiting Not Applicable

Who may 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 might be able to join this trial:

  • People who have been diagnosed with major depressive disorder (a serious form of depression, without psychosis) — either a first episode or a recurring condition — according to standard psychiatric guidelines (DSM-5)
  • People whose depression is rated as moderately severe or above on a standard depression scale called the MADRS (a score of 20 or higher), and who also score above 2 on the part of that scale measuring loss of pleasure or interest
  • People who have been on a stable antidepressant medication for at least 4 weeks before joining the trial
  • People who are able to speak and read French
  • People who have signed a consent form before the trial begins

Who may not be able to join:

  • People who have a condition that affects their sense of smell — such as being born without a sense of smell, a current upper respiratory infection, nasal or sinus disease, a brain injury, or previous nasal surgery — or who have a neurological disease
  • People who have other psychiatric disorders in addition to depression, or who use substances other than tobacco
  • People who have a medical implant or metal object in their head, as these are safety concerns for the brain stimulation treatment (TMS) used in this trial
  • People who are pregnant or breastfeeding (this is checked using a urine pregnancy test)
  • People who are under a legal protection or guardianship order (confirm with trial site)

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 28 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: BRUNELIN JEROME, PhD, hospital le vinatier

Phone: 0437915531

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
Hôpital le Vinatier
Registry
ClinicalTrials.gov
Start date
27 January 2024
Est. completion
27 January 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Change in MADRS score before and after intervention to characterized the number of depressed patients who reach remission criteria (MADRS ≤ 10) in each group

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: 28 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