Brain scans reveal how placebo cream eases pain
NCT ID NCT04653064
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study uses brain scans to explore how a placebo cream affects pain perception across different body sites. Researchers will apply a cream described as pain-relieving (though it is just a scrub) to healthy volunteers and measure their pain responses to heat. The goal is to understand how the brain represents pain and how placebos can reduce it, which may inform future non-drug pain treatments.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- placebo cream (exfoliating skin scrub)
- What this could lead to
- If successful, this could improve understanding of how placebos reduce pain, potentially leading to better non-drug pain management strategies.
- What could go wrong
- This is an early-stage, small study focused on brain mechanisms, not a treatment trial. The placebo effect is well-known but often inconsistent, and results may not translate to real-world pain relief.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2021
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subject must be a volunteer with a minimum age of 18 years and must be able and willing to provide written informed consent. * If female, the subject must be non-lactating, not pregnant, and using a reliable contraception method. * Subject must be able to read and speak English. * Subject must be able to understand and follow the instructions of the investigator and understand all screening questionnaires. * Subject must have no current or recent history of pathological pain. * Subject must have abstained from alcohol and substance use for 48 hours. * Subject must pass all fMRI screening tests. Exclusion Criteria: * If female, pregnancy. * Inability to tolerate the scanning procedures (e.g., claustrophobia). * Metal in body or prior history working with metal fragments (e.g., as a machinist). * Inability to tolerate heat pain applied to the forearm. * Reporting temporary abnormal levels of pain. * Allergic response to the exfoliating cream. * Current presence of pain. * Current or past history of psychoactive substance abuse or dependence. * Dementias. * Movement disorders except familial tremor. * CNS infection. * CNS vasculitis. * Inflammatory disease or autoimmune disease. * CNS demyelinating disease (e.g. multiple sclerosis). * Space occupying lesions (mass lesions, tumors). * Congenital CNS abnormality (e.g. cerebral palsy). * Seizure disorder. * History of closed head trauma with loss of consciousness. * History of cerebrovascular disease (stroke, TIAs). * Abnormal MRI (except changes accounted for by technical factors or UBOs. * Neuroendocrine disorders (e.g., Cushings disease). * Uncorrected hypothyroidism or hyperthyroidism. * Current or past history of cancer. * Recent history (within two years) of myocardial infarction, severe cardiovascular disease, or currently active cardiovascular disease (e.g. angina, cardiomyopathy). * Uncontrolled hypertension or hypotension. * Chronic pain syndromes. * Chronic fatigue syndromes. * A history of neurologic disease or neuropathic pain. * Prior treatment within the last month with any of the following: antidepressants, mood stabilizers, glucocorticoids, opiates. * Prior treatment with any of the following: antipsychotics, isoniazid, centrally active antihypertensive drugs (e.g. clonidine, reserpine). * Any other contraindications for MRI examination (e.g., metallic implants such as pacemakers, surgical aneurysm clips, or known metal fragments embedded in the body). * Current treatment for psychiatric disorders including mood, anxiety, substance abuse, attention-deficit/hyperactivity disorder (ADHD), psychosis. * Neurological disorders (e.g., taking dopamine agonists for Parkinson's) Cardiovascular disease or medication (e.g., taking ACE (angiotensin-converting-enzyme) inhibitors for cardiac remodeling). * Frequent smoking (\> 5 cigarettes / day). * Frequent alcohol use (\> 14 drinks / week). * Frequent migraines (\> 5 / month on average).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Dartmouth College
RECRUITINGHanover, New Hampshire, 03755, United States
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