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Lysergic Acid Diethylamide (LSD) in Palliative Care

Study acronym: LPC
StatusRecruiting
PhasePhase 2
Started
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Record History

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  1. Minor Collaborators: 2 to 3v10
  2. Minor Study sites: 3 to 4
    • Eligibility criteria expanded, about 136 words
    v9
  3. Minor Site details revised at 1 of 3 sitesv8
  4. Minor Site details revised at 1 of 3 sitesv7
  5. Minor Study sites: 2 to 3v6 Show 4 more changesShow less
    • Study completion date: Sep 2027 to May 2028
    • Start date: Jun 11, 2024 to Jun 9, 2024
    • Eligibility criteria expanded, about 9 words
    • Collaborators: 1 to 2
Show 4 earlier versionsHide 4 earlier versions
  1. Minor Start date changed from estimate of May 2024 to Jun 11, 2024v5
  2. Notable Start date: Mar 2024 to May 2024v4
  3. Notable Start date: Sep 2023 to Mar 2024v3
  4. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 2
    v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Background: Terminally ill patients often experience significant psychosocial distress having depressed mood, death anxiety, pain, and an overall poor quality of life. Recent evidence from pilot studies suggests that serotonergic hallucinogens including lysergic acid diethylamide (LSD) and psilocybin produce significant and sustained reductions of depressive symptoms and anxiety, along with increases in quality of life, and life meaning in patients suffering from life-threatening diseases. Additionally, serotonergic hallucinogens may produce antinociceptive effects. Objective and Design: The study aims to evaluate effects of LSD on psychosocial distress in 60 patients suffering from an advanced or end-stage fatal disease with a life expectancy ≥12wks and ≤2yrs in an active placebo-controlled double-blind parallel study. Patients will be allocated in a 2:1 ratio to one of the two intervention arms receiving either two moderate to high doses of LSD (100 µg and 100 µg or 100 µg and 200 µg) as intervention and two low doses of LSD (25 µg and 25 µg) as active-placebo control.
Trial Details
NCT Number NCT05883540
Lead Sponsor University Hospital, Basel, Switzerland
Collaborators: University Hospital, Zürich, Spital Uster AG, Uster, Switzerland, University Hospital, Geneva
Conditions
(from sponsor)
Palliative Care, Pain, Anxiety, Depression, Demoralization, Psychological Distress, Quality of Life, Caregiver Burden +2 more
Related terms Anxiety Disorders, Caregiver Burden, Depression, Necrophobia, Pain
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov