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Not yet recruitingNCT06558357RHUMATEPUpdated Aug 20, 2024

Diagnostic Performance of 18-FDG PET-CT Scores for the Diagnosis of Polymyalgia Rheumatica

An observational study in Inflammatory Rheumatism, 18-FDG and Positron-emission Tomography, sponsored by University Hospital, Brest. Not yet recruiting at 1 site in France. Open to participants aged 18 Years to 110 Years. Per ClinicalTrials.gov, last updated 2024-08-20.

Sponsored by University Hospital, Brest · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 10 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
210
Ages
18 Years to 110 Years
Sex
All
01

Study summary

Study of the diagnostic performance of 18-FDG PET scores in Polymyalgia rheumatica and comparaison with others inflammatories diseases.

Read the detailed description

Polymyalgia Rheumatica is difficult to diagnostic because symptoms are non specific and many diseases can be differential diagnosis (cancer, infections, others rheumatisms...).

PET-CT is more often used to help for diagnostic of inflammatory disease, and particularly inflammatory rheumatism.

Some scores have been described to harmonize the diagnosis of Polymyalgia rheumatica.

The aim of this study is to evaluate the diagnostic performance of 18-FDG PET scores in Polymyalgia rheumatica and compared with others inflammatories diseases such as ankylosing spondylarthritis.

This is a multicentric retrospective study.

02

Conditions studied

  • Inflammatory Rheumatism
  • 18-FDG
  • Positron-emission Tomography

Keywords

  • Polymyalgia rheumatica
  • FDG
  • PET
  • Diagnostic performance
  • score
03

In context

Rheumatic Fever

55 studies on the registry are indexed under Rheumatic Fever; 21 are open to participants now.

This study's planned enrollment of 210 is below the median of 300 across 26 observational studies indexed under Rheumatic Fever.

Browse Rheumatic Fever studies →

Lead sponsor

University Hospital, Brest is the lead sponsor of 601 studies on the registry; 136 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 110 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult with inflammatory rheumatism confirmed by specialist, with or without treatment and having a 18-FDG-PET CT.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Having 18-FDG PET-CT between 2012 and 2024
  • Diagnosis of inflammatory rheumatism by specialist doctor
  • Adult without opposition to use there data for research
  • Affiliate to social security system

Exclusion criteria

Exclusion Criteria:

  • Refusal participation
  • Patient under juridic protection
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
210 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Diagnostic performance of 18-FDG PET scores for diagnostic of Polymyalgia rheumatica.

    Evaluation of the metabolism of mains joints compared to liver. Calculation of different scores described in literature.

    Time frame: up to 9 months

Secondary outcomes

  1. Analysis of SUV and visual fixation of mains joints.

    Measure of SUV of mains joints and evaluation of the fixation compared to liver.

    Time frame: up to 9 months

  2. Diagnostic performance of 18-FDG PET scores for diagnostic of others inflammatory rheumatism.

    Evaluation of the precedent scores for diagnosis of others rheumatisms. Creation of others scores if some joints seem to be interesting.

    Time frame: up to 9 months

  3. Comparaison of scores with clinical, biological and radiological data.

    Search for correlation between scores and symptoms, blood test or CT/MRI exams.

    Time frame: up to 9 months

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes — All collected data that underlie results in a publication

Supporting information: Study protocol

Time frame: Data will be available beginning three years and ending fifteen years following the final study report completion

Access criteria: Data access requests will be reviewed by the internal committee of Brest UH. Requestors will be required to sign and complete a data access agreement

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 20, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06558357
Responsible party
Sponsor
First posted
Aug 16, 2024
Start date
Sep 1, 2024 (estimated)
Primary completion
Dec 31, 2024 (estimated)
Completion
Dec 31, 2024 (estimated)
Last update
Aug 20, 2024

Study contacts

Solène QUERELLOU
Contact
solene.querellou@chu-brest.fr
0298223080 ext. +33
Chloé QUERE
Contact
chloe.quere@chu-brest.fr
Solène QUERELLOU
study director · CHU Brest

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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