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Enrolling by invitationNo phase
Rubidium-82 scan to find parathyroid adenomas in primary hyperparathyroidism
Looks at how parathyroid adenomas take up rubidium-82 on PET/CT scans.
Key facts
- Who runs it
- Matthieu Pelletier-Galarneau, MD MSc
- Where
- Canada2 sites in 1 countryChoose a country to see its sites
- Trial code
- Registry title
- Parathyroid Adenoma Detection With Rubidium-82 Imaging
- Status
- Enrolling by invitation
- People taking part
- 20 people, planned
- Started
- Nov 2026
- Expected to end
- Sept 2028
- Type of study
- Observational
- Treatments tested
- PET/CT imaging with rubidium-82
- Record updated
- 27 October 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with primary hyperparathyroidism and a known parathyroid adenoma (a benign growth in a parathyroid gland). It tests whether rubidium-82 PET/CT scans can show these growths.
- Age
- 18 years or older
- Sex
- All sexes
- Disease stage
- Primary hyperparathyroidism shown by blood tests, with a parathyroid adenoma. People with normal calcium levels (normocalcemic form) cannot join.
- Earlier treatment
- A parathyroid adenoma must already have been seen on an earlier 18F-fluorocholine scan.
- Biomarker or test result
- Blood test results showing primary hyperparathyroidism.
Main reasons for not taking part
- Primary hyperparathyroidism with normal calcium levels
- Pregnancy or breastfeeding
- Fear of closed spaces, or not able to go through the scans
- Other illness or condition that the study doctor thinks would affect taking part
The registry criteria, word for word
Show all 9 criteriaShow less
Who can take part
- Age ≥ 18y
- Ability to undergo imaging logistics
- Ability to provide informed consent
- Biochemical evidence of primary hyperparathyroidism
- Documented parathyroid adenoma on prior 18F-fluorocholine imaging
Who cannot take part
- Any other history, condition, therapy, or uncontrolled intercurrent illness, which could in the opinion of the investigator affect compliance with study requirements or which would make the participant unsuitable for this study
- Normocalcemic primary hyperparathyroidism
- Breastfeeding or pregnancy
- Claustrophobia or inability to undergo imaging logistics
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
Assess the uptake of rubidium-82 in parathyroid adenomas.
Treatments tested
- PET/CT imaging with rubidium-82
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Parathyroid Adenoma Detection With Rubidium Chloride Imaging: A Proof-of-Concept Study
- Plain-language title
- Rubidium-82 scan to find parathyroid adenomas in primary hyperparathyroidismGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 15 November 2026.
- Record updated
- 27 October 2026