ClinicalTrials.gg
RecruitingNCT07914179InfraAJIUpdated Nov 3, 2026

The Use of Infrared Cameras for Detecting Juvenile Idiopathic Arthritis

An interventional study of standardized evaluation and single IRT session and a minimal blood test in Juvenile Idiopathic Arthritis, Infrared Thermography and Joint Inflammation, sponsored by Centre Hospitalier Universitaire, Amiens. Recruiting at 1 site in France. Open to participants aged 2 Years to 16 Years. Per ClinicalTrials.gov, last updated 2026-11-03.

Sponsored by Centre Hospitalier Universitaire, Amiens · Not applicable, Interventional, and Screening

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Updated Nov 3, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Non-randomized
Ages
2 Years to 16 Years
Sex
All
01

Study summary

Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disease in children, causing persistent joint inflammation, pain, and functional impairment. Current monitoring relies on clinical scores, laboratory markers, and imaging, which are often resource intensive. Infrared thermography (IRT) is a non-invasive, radiation-free method that detects skin temperature changes potentially reflecting joint inflammation. Evidence in pediatric populations is limited, but IRT could provide an objective, reproducible, and child-friendly tool. This study aims to evaluate IRT's diagnostic accuracy by comparing it with clinical scores, laboratory markers, and ultrasound Doppler, to assess its utility as a complementary monitoring tool.

Patients with JIA will undergo clinical examination, routine blood tests, and IRT at baseline, 1 month, and 3 months. Control patients will participate in a single IRT session and, a CRP/ESR/blood test; if a biological workup is already planned as part of their routine care, existing results will be collected, and no additional sampling will be performed. IRT will follow a standardized protocol, including an acclimatization period, predefined positioning, and acquisition of three consecutive images per joint. After completion of the study, JIA patients will resume their standard-of-care follow-up.

02

Conditions studied

  • Juvenile Idiopathic Arthritis
  • Infrared Thermography
  • Joint Inflammation
  • Diagnostic Imaging
  • Pediatrics

Keywords

  • Juvenile idiopathic arthritis
  • Infrared thermography
  • Joint inflammation
  • Diagnostic imaging
  • Pediatrics
  • Case-control study
03

In context

Arthritis, Juvenile

365 studies on the registry are indexed under Arthritis, Juvenile; 101 are open to participants now.

This study's planned enrollment of 60 is above the median of 52 across 230 interventional studies indexed under Arthritis, Juvenile.

Browse Arthritis, Juvenile studies →

Lead sponsor

Centre Hospitalier Universitaire, Amiens is the lead sponsor of 586 studies on the registry; 185 are open to participants now.

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

04

Who can participate

Ages eligible
2 Years to 16 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  • children aged 2-16 years with clinically suspected arthritis affecting the knee, ankle, wrist, or hand, irrespective of disease stage,
  • control group : children with non-inflammatory conditions and no history of or inflammatory disease.

Exclusion criteria

Exclusion Criteria:

  • other inflammatory or non-inflammatory diseases or recent trauma/surgery explaining joint symptoms,
  • local skin conditions interfering with infrared imaging, and treatments or comorbidities likely to alter joint or body temperature.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Patients with JIA

    Other: standardized evaluation

  • Active comparator
    Control patients

    Other: single IRT session and a minimal blood test

Interventions

  • Otherstandardized evaluation

    Patients with JIA will undergo a standardized evaluation including a clinical joint examination, routine blood tests (CRP, NFS, ionogram, liver function, coagulation), and IRT of selected joints

  • Othersingle IRT session and a minimal blood test

    Control patients will undergo a single IRT session and a minimal blood test (CRP, ESP, blood count). IRT will be performed under controlled conditions with a defined joint positioning, 15-30 minutes of acclimatization, and acquisition of three consecutive images per joint.

06

What researchers measure

Primary outcomes

  1. variation of IRT measure between both groups

    variation of IRT measure between both groups

    Time frame: at baseline

  2. variation of IRT measure between both groups

    variation of IRT measure between both groups

    Time frame: at 1 month

  3. variation of IRT measure between both groups

    variation of IRT measure between both groups

    Time frame: at 3 months

Secondary outcomes

  1. longitudinal changes in thermographic measurements

    longitudinal changes in thermographic measurements by comparing temperature differences (ΔT) between baseline (D0) and 3 months

    Time frame: at 3 months

  2. correlation of longitudinal changes in thermographic measurements with clinical parameters

    Time frame: at 3 months

  3. correlation of longitudinal changes in thermographic measurements with functional parameters

    Time frame: at 3 months

  4. correlation of longitudinal changes in thermographic measurements with biological parameters

    Time frame: at 3 months

  5. correlation of diagnostic performance of IRT with clinical examination

    Time frame: at 3 months

  6. correlation of diagnostic performance of IRT with ultrasounds

    Time frame: at 3 months

  7. correlation of diagnostic performance of IRT with MRI

    Time frame: at 3 months

  8. reproducibility of IRT measurements

    Time frame: at 3 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Aug 2026 (actual). Primary completion is estimated for Aug 2028, 24 months after the start.

Of 53 non-industry interventional studies with no phase under Arthritis, Juvenile, half reached primary completion within 13 months of starting (the median), counting those still running; a quarter within 8 and three quarters within 35. This study's planned 24 months is above that.

Counting every sponsor, half of 56 studies reached it within 14 months; a quarter within 8 and three quarters within 39.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 13, 2026
First posted
Nov 3, 2026
StartActual
Aug 24, 2026
Primary completionEst.
Aug 2028
CompletionEst.
Oct 2028
Last update
Nov 3, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 3, 2026
Show all 1 update
  1. Nov 3, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07914179
Responsible party
Sponsor
First posted
Nov 3, 2026
Start date
Aug 24, 2026
Primary completion
Aug 2028 (estimated)
Completion
Oct 2028 (estimated)
Last update
Nov 3, 2026

Study contacts

Djamal-Dine DJEDDI, Pr
Contact
Djeddi.Djamal-Dine@chu-amiens.fr
33+322035590

Oversight

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

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