Phase 2 Depression and Anxiety Trial, Recruiting NCT06626152 Sponsor: University of British Columbia Condition: Depression and Anxiety
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Phase 2 Depression and Anxiety Trial, Recruiting

NCT06626152
Recruiting Phase 2

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:

  • You are seen as an outpatient (not currently staying in a hospital) and are able to give your own consent to participate
  • You are at least 60 years old
  • You have been diagnosed with major depressive disorder based on a structured psychiatric interview
  • Your depression has been assessed as moderate to severe using a standard rating scale (a score of 15 or higher on the MADRS)
  • You have been on a stable dose of any psychiatric medications, including antidepressants, for at least 4 weeks
  • You are able to follow the study schedule and attend appointments as required

Who may not be able to join:

  • You have been diagnosed with a major neurocognitive disorder (such as dementia)
  • You are currently experiencing psychosis (such as hallucinations or delusions)
  • You have an unstable or poorly controlled medical condition affecting your heart, hormones, blood, liver, lungs (including asthma), or kidneys
  • You have been diagnosed with a specific type of eye condition called narrow angle glaucoma
  • You have unexplained skin lesions that have not been checked, or you have a history of melanoma (a type of skin cancer)
  • You have had a heart attack at any point in the past
  • You have a heart rhythm problem affecting the upper or lower chambers of your heart
  • You have a history of seizures or a seizure disorder (such as epilepsy)
  • You have a history of peptic ulcer disease (stomach or intestinal ulcers)
  • You have had an allergic or sensitivity reaction to levodopa, carbidopa, or any ingredient in the study medication (Levocarb)
  • You are currently having thoughts of suicide
  • Your psychiatric medication was started or the dose was changed less than 4 weeks before joining the trial
  • You regularly take medications that block dopamine, or regularly use sedative medications (benzodiazepines) at a dose of 2mg lorazepam equivalent or more per day
  • You are unable to complete memory and thinking tests conducted in the English language
  • You have a significant problem with your hearing or vision that cannot be corrected well enough to complete the thinking and memory tests
  • You have been falling frequently, with one or more falls per week over the past 4 weeks

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 5 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 6048069090

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
Phase 2
Registry
ClinicalTrials.gov
Start date
15 August 2024
Est. completion
30 May 2026

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

L-DOPA challenge completion rate; Depressive symptoms; Gait speed; Psychomotor speed

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: 5 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