Actively Recruiting
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
Eligibility Criteria
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
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
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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