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Brain scans reveal Dopamine's role in chronic pain

NCT ID NCT05285683

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study explores how dopamine, a brain chemical linked to motivation, influences chronic pain. Ten adults with chronic pain will receive two dopamine-boosting drugs (methylphenidate and carbidopa-levodopa) or a placebo, then undergo brain scans to measure changes in key pain-related areas. The goal is to understand the brain's pain signature, not to treat pain directly.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
methylphenidate and carbidopa-levodopa
What this could lead to
If successful, this could reveal how dopamine influences chronic pain in the brain, pointing toward new treatment targets.
What could go wrong
This is a very small early-phase study with only 10 participants, focused on brain changes rather than pain relief, so results may not lead to treatments.

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

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

About 10 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2024

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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: The following inclusion criteria must be met for all subjects to be considered eligible to participate: 1. 18 years old or older 2. Equal numbers of men and women, as well as racial and ethnic makeup representative of surrounding area 3. Able to speak, read, and understand English 4. In generally stable health 5. Sign informed consent document The following inclusion criteria must be met for chronic pain patients to be considered eligible to participate: 1. Patients must report chronic pain for more than 1 year. 2. The reported pain should be rated at ≥ 40/100 Exclusion Criteria: General exclusion criteria for all subjects include: 1. Significant other medical disease, such as unstable diabetes mellitus, congestive heart failure, coronary or peripheral vascular disease, chronic obstructive lung disease, or malignancy 2. History of traumatic brain injury (TBI) 3. Current misuse/dependence on substance(s), including alcohol, at the time of study enrollment 4. Major psychiatric disorder during the past 6 months 5. Significantly abnormal laboratory values, which include, but are not limited to, the following: 1. White blood cell (WBC) \< 1.5 or \>15.0 x 10\^3/μL 2. Hemoglobin (Hgb) \< 8 gm/dL 3. Hematocrit (Hct) \< 24% or \> 50% 4. Platelets (Plts) \<50 or \> 1000 x10\^3 5. Creatine \> 2 mg/dL 6. Glucose \> 125 mg/dL 7. Aspartate aminotransferase (AST) \> 250 U/L 8. Alanine Transaminase (ALT) \> 250 U/L 9. Bilirubin \> 3 mg/dL 6. Intra-axial implants (e.g. - spinal cord stimulators or pumps) 7. Inability to adequately perform the finger-span visual tracking task (training for rotating pain perception, see Brain Imaging Details). 8. All MRI exclusionary criteria: any metallic implants, brain or skull abnormalities, tattoos on large body parts, pregnancy, and claustrophobia. 9. In the judgement of the investigator, unable or unwilling to follow the protocol and instructions. 10. Gambling addiction self-reported during screening process (ensure computer-based games do not cause psychological or emotional problems) 11. Chronic pain patients with past history of allergic reactions to methylphenidate or levodopa/carbidopa. For healthy control subjects, current complaint(s) of pain, or a history of pain lasting \>4 weeks in the last year, will be excluded from participating. In addition, exclusion criteria for chronic pain subjects also includes: 1. Pain that is associated with any systemic signs or symptoms (e.g. - fever, chills) 2. Evidence of rheumatoid arthritis, ankylosing spondylitis, acute vertebral fractures, fibromyalgia, history of tumor(s) in the back. 3. Involvement in litigation regarding their pain, or having a disability claim, or receiving workman's compensation, or seeking either because of their pain. 4. Treated with methadone for opioid use disorder (i.e. - not just for pain)

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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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • University of Rochester Medical Center

    RECRUITING

    Rochester, New York, 14642, United States

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