Skip to main content

LSD-Assisted Therapy protocol

Compound: LSD

Status: research

Classic psychedelic being revisited for anxiety and addiction

Dosing

Dose: 25 to 200 micrograms in modern controlled studies; 100 micrograms in the 2024 GAD Phase 2b

Route: Oral, in trials

Duration: 8 to 12 hours

Sessions: Single or spaced sessions per protocol

Safety

Monitoring: Continuous supervision through the session, blood pressure checks, calm containment for difficult periods rather than premature chemical intervention where clinically appropriate.

Side effects

  • Anxiety waves during the session
  • Elevated heart rate and blood pressure
  • Perceptual after-effects
  • Rare persistent perceptual changes

Contraindications

  • Psychosis or mania history
  • Lithium use
  • Significant cardiovascular disease
  • Unstable psychiatric presentation
  • Pregnancy

Overview

Mechanism: LSD is a long-acting serotonin 2A receptor agonist producing 8 to 12 hours of altered perception, cognition, and affect. Modern trials focus on anxiety and depression.

Indications

  • Under clinical investigation for generalized anxiety disorder and depression
  • Historical research in anxiety associated with serious illness

Evidence level: A Phase 2b trial of a single 100 microgram dose for generalized anxiety disorder reported significant improvement, and the program received US FDA breakthrough therapy designation in 2024. Earlier controlled work includes LSD-assisted psychotherapy for end-of-life anxiety.

Citations

Doi: 10.1097/NMD.0000000000000113

Year: 2014

Title: LSD-assisted psychotherapy for anxiety associated with a life-threatening disease: a randomized active placebo pilot study

Year: 2024

Title: Phase 2b trial of MM120 (lysergide) for generalized anxiety disorder; FDA breakthrough therapy designation

Integration

Prompts

  • Which hour of the session mattered most and why?
  • What changed in how the anxiety is held?
  • Any visual forms worth documenting to the registry standard?

Framework: Next-day and one-week integration sessions in trial protocols, with standard scales tracking anxiety and mood. The long arc of the session tends to produce a large amount of material; integration prioritizes rather than exhausts it.

Preparation

Screening

  • Psychiatric screening for psychosis, mania, and family history
  • Cardiovascular screening
  • Medication review including lithium, which is dangerous in combination
  • Session-day logistics: the duration requires a full supervised day

Set setting: Clinical settings with trained monitors for the full duration, comfortable room, music and eyeshades optional, no driving until fully recovered.

Legal status: LSD is a Schedule I controlled substance in the United States and controlled internationally. Swiss compassionate-use programs have allowed limited supervised clinical use. Reference material, not medical advice.

Reference material only. Nothing on this page is medical advice or a personal recommendation.

Back to the protocol catalogue