Phase 4 Depression and Anxiety Trial, Recruiting NCT03272698 Sponsor: University of Saskatchewan Condition: Depression and Anxiety
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Phase 4 Depression and Anxiety Trial, Recruiting

NCT03272698
Recruiting Phase 4

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 a depression severity score above 20 on a standard rating scale called the MADRS, and who are already planned to receive electroconvulsive therapy (ECT)
  • People whose depression meets the definition of treatment-resistant depression (TRD), meaning at least two standard antidepressant medications have been tried for an adequate length of time without sufficient improvement

Who may not be able to join:

  • People who are unable to give informed consent to participate in the trial
  • People whose overall physical health is rated at a high-risk level (a score of 4 or above on a scale used by anaesthesiologists to assess surgical risk)
  • People who have an implanted electronic medical device, such as a pacemaker, defibrillator, spinal cord stimulator, deep brain stimulator, or implanted drug pump
  • People who have a diagnosis of schizoaffective disorder
  • Women who could potentially become pregnant and either decline a urine pregnancy test or receive a positive result on that test
  • People who have a known allergy to any of the study medications or their ingredients
  • People with a serious physical health condition that the treating psychiatrist or anaesthesiologist considers to be a reason to avoid ECT — this includes certain heart conditions (such as uncontrolled high blood pressure), breathing problems, brain or blood vessel conditions, raised pressure inside the skull (including glaucoma), or a history of seizures

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 15 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Principal Investigator: Jonathan Gamble, MD, University of Saskatchewan

Phone: 3066551183

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 4
Sponsor
University of Saskatchewan
Registry
ClinicalTrials.gov
Start date
1 September 2017
Est. completion
31 December 2025

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Number of treatments required to reach disease remission

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: 15 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