Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06368492

The Impact of Psilocybin on Pain in Fibromyalgia Patients

Led by Maastricht University · Updated on 2025-09-15

35

Participants Needed

2

Research Sites

82 weeks

Total Duration

On this page

Sponsors

M

Maastricht University

Lead Sponsor

L

Leiden University Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

Rationale: Recent evidence shows that Lysergic Acid Diethylamide (LSD), even when administered in low, non-hallucinogenic doses, can produce analgesic effects and improve pain tolerance in a sample of healthy volunteers. Such results complement what was already observed with other serotonergic psychedelics such as psilocybin: survey studies and case series indicate that its use may lead to improvements in chronic pain conditions such as migraines, cluster headaches and phantom limb pain even at low, non-psychedelic doses. These effects have however not yet been investigated and confirmed in clinical populations under controlled experimental conditions. Fibromyalgia (FM) is a chronic condition characterised by widespread pain, hyperalgesia, anxiety, disturbed sleep patterns, impaired cognitive functioning and comorbid mood disorders. Most suggested therapies are only associated with small improvements in pain ratings and quality of life. Currently, there is no data concerning the effectiveness of serotonergic psychedelics in improving pain ratings in fibromyalgia patients. Objective: The present study will explore the effects that the administration of a placebo and 2 low psilocybin doses (5 mg or 10 mg) will have on pain perception in a group of fibromyalgia patients. Study design: The present study uses a double-blind, randomized, placebo-controlled design. All participants will receive a placebo and 2 doses of psilocybin (5 mg or 10 mg) and will undergo the Cold Pressor Test (CPT) and the Pain Pressure Threshold Task (PPT) o test its analgesic effects.

CONDITIONS

Official Title

The Impact of Psilocybin on Pain in Fibromyalgia Patients

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65 years
  • Body mass index (weight/height2) between 18 and 28 kg/m2
  • Diagnosis of fibromyalgia according to American College of Rheumatology criteria
  • Minimum pain score of 5 out of 10 on the Numeric Rating Scale
  • Proficient in Dutch or English language
  • Provided written informed consent
  • Understand the study procedures and risks
  • No regular use of psychotropic medications such as opiates, antidepressants, muscle relaxants, anticonvulsants, sleep aids, or benzodiazepines
  • Allowed use of non-pharmacological treatments and one rescue therapy: acetaminophen ≤4,000 mg/day, ibuprofen ≤1,200 mg/day, naproxen ≤660 mg/day, or ketoprofen ≤75 mg/day
  • Willingness to avoid psychoactive substances during the study
  • Willingness to drink only alcohol-free liquids and avoid coffee, black or green tea, or energy drinks after midnight before study sessions and during study days
  • Willingness not to drive or operate machinery within 24 hours after substance administration
Not Eligible

You will not qualify if you...

  • Presence of other painful conditions such as inflammatory rheumatic diseases, migraines, or headaches
  • Presence or history of psychiatric conditions including major depressive disorder, anxiety disorders, or substance use disorder
  • Previous serious side effects to psychedelic drugs such as anxiety or panic attacks
  • Tobacco smoking more than 20 cigarettes per day
  • Excessive alcohol consumption over 20 drinks per week
  • Psychotic disorder in first-degree relatives
  • Pregnancy or lactation
  • High blood pressure (diastolic > 90 mmHg; systolic > 140 mmHg)
  • History of cardiac problems like arrhythmia or ischemic heart disease
  • For women, not using a reliable contraceptive method

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Maastricht University

Maastricht, Limburg, Netherlands, 6226AK

Actively Recruiting

2

Leiden University Medical Center

Leiden, South Holland, Netherlands, 2333

Actively Recruiting

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Research Team

M

Mauro Cavarra, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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