New scan aims to reveal hidden source of Post-Surgery pain
NCT ID NCT06171659
First seen Jun 25, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This study is testing whether a combined PET and MRI scan, using a radioactive tracer called FDG, can accurately locate the source of chronic pain that persists after joint surgery. Researchers will scan 128 people with and without pain to see if the scan can spot where pain is coming from. If it works, it could help doctors treat chronic pain more effectively by targeting the right area.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- FDG radiotracer (a radioactive sugar used for imaging)
- What this could lead to
- If successful, this could give doctors a reliable way to pinpoint the exact cause of chronic pain after surgery, leading to more targeted and effective treatments.
- What could go wrong
- This is an early-stage imaging study, not a treatment trial. It may not find a clear pain source in all patients, and the results may not change how pain is managed in practice.
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.
- Participants
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About 128 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2024
- Expected to finish
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Jun 2028
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.
Who is studied
Participants with persistent post-surgical pain and asymptomatic individuals who have undergone joint arthroplasty (hip or knee) or joint arthroscopy (hip or knee).
- Ages
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18 to 85 years
- 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: Persistent Post-Surgical Pain Patients * 18-85 years old * Presents with persistent pain with pain score of ≥4 on Numerical Rating Scale \[0:10\] for at least 6 months following joint arthroplasty or arthroscopy. * Able and willing to provide informed consent * Willing and able to undergo PET/MRI (arthroplasty and arthroscopy participants) and PET/CT (arthroplasty participants only) Inclusion Criteria: Asymptomatic controls * 18-85 years old * Asymptomatic (pain score of ≤2 on the NRS) for at least 6 months following joint arthroplasty or arthroscopy. * Able and willing to provide informed consent * Willing and able to undergo PET/MRI Exclusion Criteria: * Inability to understand and communicate with the investigators to complete the study-related questionnaires. * Any co-morbidity which results in severe systemic disease limiting function as defined by the American Society of Anesthesiology (ASA) physical status classification \> 3, such as the presence of current or past (6 months) pulmonary, hepatic, renal disease, arthritis, hematopoietic, and neurological diseases not related to chronic pain. * Pregnant or breastfeeding. (Individuals with childbearing potential will be asked to verbally confirm they are not pregnant. If they cannot confirm, they will have a urine pregnancy test either at the imaging study visit or within 7 days prior to the imaging study visit.) * Subject with contraindication(s) to or inability to undergo PET/MRI * Current diagnosis of malignancy of any kind. Participants in remission for at least two years and not undergoing any treatment may be considered per investigator discretion * Current enrollment in a scientific interventional or treatment study. * Subject unable or unwilling to provide informed consent
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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 study's own enquiry address
This study publishes an address for enquiries. See it below .
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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
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Contacts and locations
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Study contacts
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Contact
Email: •••••@•••••
Locations
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UW School of Medicine and Public Health
RECRUITINGMadison, Wisconsin, 53792, United States
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