Phase 2 Peripheral Neuropathy Trial, Recruiting NCT06731335 Sponsor: Unity Health Toronto Condition: Peripheral Neuropathy
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Phase 2 Peripheral Neuropathy Trial, Recruiting

NCT06731335
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 between 18 and 65 years old
  • A pain specialist has diagnosed you with long-lasting nerve pain (chronic neuropathic pain)
  • Your nerve pain is rated as moderate to severe based on a standard patient questionnaire
  • You have already tried at least two medications recommended in Canadian guidelines for nerve pain, and did not feel they meaningfully helped your symptoms
  • You have a good enough understanding of English to take part in talk therapy (psychotherapy)
  • If you are able to become pregnant, you are willing to use a highly effective or double-barrier form of birth control during the trial

Who may not be able to join:

  • You have a history of addiction to or misuse of the drug Dextromethorphan
  • A genetic test shows that your body is unable to process certain medications through a specific enzyme called CYP2D6 (confirm with trial site)
  • You have certain mental health conditions, including a personal or family history of psychosis, bipolar disorder, borderline personality disorder, paranoid personality disorder, current thoughts of suicide, or a substance use problem within the past 12 months
  • You are currently taking medications that may interact with the drugs used in this study (confirm with trial site)
  • You have an unstable or poorly controlled medical condition, such as heart disease, liver disease, or severe kidney disease
  • You have ever previously used a psychedelic drug that affects serotonin (such as psilocybin or LSD)
  • You are currently pregnant or breastfeeding
  • You have any other significant health condition that the study doctor believes could affect the results or put your health at risk

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 19 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Unity Health Toronto
Registry
ClinicalTrials.gov
Start date
5 March 2025
Est. completion
1 August 2026

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Feasibility to recruit 30 participants into a trial of psilocybin and active placebo to prepare for a larger multicentre trial

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: 19 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