Skip to content

Evaluating the Potential of Microdosing 1cp-LSD for the Treatment of Canine Anxiety: A One-Month Case Study.

Elisa Hernández-Álvarez, Lucas F Borkel, Jaime Rojas-Hernández, Domingo J Quintana-Hernández, Ignacio García-Serrano, Tobías Fernández-Borkel, Manuel Zumbado, Luis Alberto Henríquez-Hernández

Veterinary medicine and science July 1, 2025 DOI: 10.1002/vms3.70486 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Pilot study, single-case study Case report Peer reviewed
Sample size 1
Population A 13-year-old female dog with severe separation anxiety
Intervention 1cp-LSD
Dose 5 µg every 3 days
Duration 1-month treatment, 1-month follow-up
Topics Anxiety LSD Microdosing
Keywords 1cp‐LSD Animal behaviour Animal consciousness Dogs Microdosing: microdosing Psychedelic microdosing Dog anxiety Animal anxiety Psychedelics: psychedelics 1cp-LSD Psychedelic compounds Dog behavior
Citations 3
Key findings Microdosing 1cp-LSD was associated with a reduction in canine anxiety scores from severe to moderate, but the absence of a control group limits causal interpretation.

Abstract

This pilot study explored the potential of microdosing 1-cyclopropionyl-d-lysergic acid diethylamide (1cp-LSD) to treat canine anxiety. A single-case study was conducted on a 13-year-old female dog with severe separation anxiety, who was treated with 5 µg of 1cp-LSD every 3 days for a month. Anxiety was assessed before, after, and 1 month following treatment using a validated questionnaire. The owner's attachment style was assessed using a validated scale. The dog's anxiety score significantly decreased from 29 (severe) to 14 (moderate) after treatment. A reduction in anxiety levels was observed, characterized by decreased destructive behaviour and shorter durations of vocalization. This improvement was sustained 1 month following treatment, although vocalization frequency increased. These findings suggest potential therapeutic efficacy of microdosing 1cp-LSD in managing canine anxiety; however, the absence of a control group makes it difficult to determine whether the observed effects are due to 1cp-LSD, owner bias, or natural variability in the dog's behaviour. Additional studies with blinded protocols and larger sample sizes are necessary to validate these findings and further explore the impact of owner attachment on canine anxiety.

Comparable studies

Other non-randomized and open-label trials on LSD and microdosing, most cited first.

Study Year Design Participants
An open-label pilot trial assessing tolerability and feasibility of LSD microdosing in patients with major depressive disorder (LSDDEP1). Patients with major depressive disorder meeting DSM-5 criteria 2023 Open-label pilot trial n = 20
LSD microdosing in major depressive disorder: results from an open-label trial Participants with major depressive disorder, most taking antidepressant medication 2025 Open-label phase 2A trial n = 19
LSD microdosing for major depressive disorder: Mood and pharmacokinetic outcomes from a Phase 2a trial People with depression 2026 Clinical trial
What is it like to microdose LSD for depression? a thematic analysis of participant interviews from an open-label trial. Adults with major depressive disorder 2025 Open-label pilot trial (phase IIa) with post-intervention qualitative interviews n = 17
155. EXPLORING LSD MICRODOSING IN AN OPEN-LABEL PILOT FOR MAJOR DEPRESSIVE DISORDER: THE INTERPLAY OF BEHAVIORAL ACTIVATION, MOOD IMPROVEMENT, AND CONNECTEDNESS Individuals with major depressive disorder 2025 Open label trial n = 17

Explore topics

By condition and practice