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Giant Cell ArteritisNCT06011512

Risk of Diabetes Mellitus in Patients With Giant Cell Arthritis and Polymyalgia Rheumatica.

An observational study of Giant Cell Arteritis and Polymyalgia Rheumatica, run by Salome Kristensen at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this observational study is to expand the knowledge about development and aggreviation of diabetes mellitus in patients with giant cell arthritis and polymyalgia rheumatica. Read more about this study

Who is it for?
Ages 50 to 85 years
How many people
198 participants
Where
1 siteDenmark
Study dates
1 Aug 2023to 1 Sep 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The population from which the cohort will be selected from, are patients who are treated at their respective outpatient rheumatology clinic. At least 8 departments of rheumatlogy in Denmark are expected to include patients.

Who may be able to join

  • Men or women aged 50 to 85 years
  • Are diagnosed with GCA or PMR
  • Diagnosis is established by or confirmed by a rheumatologist (clinical expert opinion)
  • Speak and understand Danish
  • Are able to give signed and dated informed consent

Who cannot join

  • None

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Aalborg University Hospital

    Aalborg, North Denmark, 9000

Other trials in Denmark

About this study

The goal of this observational study is to expand the knowledge about development and aggreviation of diabetes mellitus in patients with giant cell arthritis and polymyalgia rheumatica.

The main questions it aims to answer are:

Read more
  • To identify the risk of comorbidities, especially diabetes, in patients with giant cell arthritis and polymyalgia rheumatica, treated with glucocorticoids in combination with or without interleukin-6 inhibitor.
  • To identify clinical outcomes and biomarkers as potential predictors for development or aggregation of already existing diabetes mellitus in patients with giant cell arthritis or polymyalgia rheumatica using machine learning prediction.

Participants will be followed at their respective rheumatology clinic, and will be asked to deliver blood samples at predefined visits.

Read the detailed description

The cohort study is a prospective national cohort study in patients with giant cell arthritis (GCA) and polymyalgia rheumatica (PMR). At baseline and follow-up visits at month 1, 3, 6, 12, and every year while patients are treated at departments of rheumatology, collection of demographics, clinical data, patient reported outcomes and blood samples (Regionernes blod- og GenomBank) will occur.

Trial procedure:

Diagnostic information and referral history:

At enrollment, patients will be registered as either incident (first visit within 3 months from diagnosis) or prevalent. The patients diagnosis, time of diagnosis, type of physician establishing diagnosis, time of symptom onset, time of referral, time of first visit, date of prednisolone start, initial prednisolone dose, basis for diagnosis (clinical, classification criteria, biochemical, ultrasound, PET/CT, other imaging modalities, temporal artery biopsy), fulfillment of 1990 ACR classification criteria for GCA, fulfillment of 2018 DCVAS classification criteria for GCA, fulfillment of 2012 EULAR PMR classification criteria will be recorded. Disease stratification will be performed according to clinical diagnosis and imaging test results available. Accordingly, patients will be categorized as either 'GCA', 'PMR', 'GCA and PMR'. If a GCA diagnosis is established, patients will be further categorized as 'c-GCA', 'LV-GCA'

Clinical evaluation:

At each visit, physician disease activity category; remission, potential relapse without treatment escalation, relapse (treatment escalation, refractory disease) will be recorded. Any relapse, that lead to treatment intensification since last study visit, will be recorded. If a relapse is suspected at the current visit, the findings supporting the suspicion of disease activity and the therapeutic consequence, will be recorded.

Demography:

The patients age, gender, height, weight and history of smoking and alcohol consumption will be recorded at enrollment.

Medication:

At each visit current dose of prednisolone, methotrexate or IL-6i treatment are recorded. Date of start and discontinuation and reason for discontinuation of immunosuppressive therapy will be recorded.

Adverse events and treatment related disease burden:

Adverse effects that cause change in treatment strategy will be recorded.

DM:

At each visit data regarding development of diabetes, aggreviation of exciting DM, HgbA1c and blood glucose will be recorded.

Patient reported outcome measures (PROMs): At each visit patients will be asked to report

  • Patient global numerical rang scale (NRS, 0-10)
  • Patient pain NRS, neck, shoulder, pelvic, thigh (0-10)
  • Patient pain NRS headache (0-10)
  • Duration of morning stiffness (minutes)
  • Morning stiffness NRS (0-10)
  • European Quality of life -5dimension5-levels (EQ-5D-5L)

Laboratory test:

Routine blood analysis, including CRP and HbA1c, will be performed as standard of care and according to the National Danish GCA and PMR management guideline [5]. At each visit, CRP will be recorded. HbA1c and time of analysis of HbA1c can be recorded at any visit. Additionally, biobank blood samples will be collected at each study visit (study-related procedure):

  • 1 × EDTA plasma tube (lavender-top), 9 ml
  • 1 × Full blood DNA, 1.5 ml
  • 2 × EDTA plasma, 2 ml
  • 1 × EDTA buffy coat,
  • 2 × serum tube (red-top), 9 ml
  • 4 × serum tube, 2 ml

Time of blood sampling will be recorded. A time frame of ± 2 weeks from time of study visit will be accepted for CRP and biobank samples. However, collection of planned blood samples at any study visit, where a relapse is suspected, is strived for before treatment escalation. Furthermore, CD36, sCD36, homeostatic model assessment for insulin resistance (HOMA-IR), proinsulin C-peptide, fasting proinsulin C-peptide and fasting blood glucose are of special interest. For a subgroup of patients, oral glucose tolerance test will be performed. Biomarkers will be analysed at Aalborg University Hospital in collaboration with department of Clinical Biochemistry. Data will be gathered from Aalborg university hospital and in order to strengthen the study, further data from other departments of rheumatology will be requested from the DANIVAS database (Danish national database of patients with GCA and PMR).

Patient data can be collected at any time during their disease course.

Type of visits performed:

  • Enrolment visit: First visit
  • Follow up visits:
  • Treatment response visit: Visits scheduled 1-2 months after treatment start or intensification to assess the effect of treatment.
  • Planned follow up
  • Suspected relapse or adverse events visit: An extra visit on the suspicion of relapse or adverse events potentially requiring treatment adjustment.
Medical subject headings
Giant Cell Arteritis, Polymyalgia Rheumatica

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proportion of participants developing diabetes mellitus during the study period, measured in changes of HbA1c.

    HbA1c is glycated hemoglobin, which means that hemoglobin is chemically bound to glucose in the bloodstream. HbA1c is a relative measure of the average glucose in the bloodstream during the past 3 months, and is used to diagnose patients with diabetes mellitus.

    Measured: At baseline, and month 1, 3, 6, 12, 24 and 36.

Secondary outcomes (13)
  1. Changes in CD36.

    CD36 is a protein that helps importing fatty acids inside the cell.

    Measured: At baseline, and month 1, 3, 6, 12, 24 and 36.

  2. Changes in sCD36.

    CD36 is a protein that helps importing fatty acids inside the cell.

    Measured: At baseline, and month 1, 3, 6, 12, 24 and 36.

  3. Changes in homeostatic model assessment for insulin resistance.

    Homeostatic model assessment for insulin resistance (HOMA-IR) is a score that approximates insulin resistance.

    Measured: At baseline, and month 1, 3, 6, 12, 24 and 36.

  4. Changes in proinsulin C-peptide.

    Proinsulin C-peptide is a marker for the insulinproduction.

    Measured: At baseline, and month 1, 3, 6, 12, 24 and 36.

  5. Changes in fasting proinsulin C-peptide.

    Proinsulin C-peptide is a marker for the insulinproduction.

    Measured: At baseline, and month 1, 3, 6, 12, 24 and 36.

  6. Changes in fasting blood glucose.

    Blood glucose is the amount of glucose in the bloodstream.

    Measured: At baseline, and month 1, 3, 6, 12, 24 and 36.

  7. Changes in CRP.

    CRP is a pro-inflammatory marker.

    Measured: At baseline, and month 1, 3, 6, 12, 24 and 36.

  8. Changes in patient pain numerical rating scale, (0-10).

    Patient pain numerical rating scale, neck, shoulder, pelvic, thigh is a rating scale in which patients are asked to rate the pain from 0 to 10 in the chosen areas, with 0 being "no pain" and 10 being "worst pain imaginable".

    Measured: At baseline, and month 12, 24, 36, 48, and 60.

  9. Changes in patient pain numerical rating scale headache (0-10).

    Patient pain numerical rating scale headache is a rating scale in which patients are asked to rate their headache pain from 0 to 10 with 0 being "no pain" and 10 being "worst pain imaginable".

    Measured: At baseline, and month 12, 24, 36, 48, and 60.

  10. Changes in duration of morning stiffness.

    With regard to duration of morning stiffness, patients are asked to rate the duration of their morning stiffness with 0 being no stiffness and 10 being 2 hours of stiffness or more.

    Measured: At baseline, and month 12, 24, 36, 48, and 60.

  11. Changes in morning stiffness numerical rating scale (0-10).

    Moring stiffness numerical rating scale is a measure of the difficulty the morning stiffness are causing, with 0 being "no difficulty" and 10 being "the worst imaginable difficulty".

    Measured: At baseline, and month 12, 24, 36, 48, and 60.

  12. Changes in European Quality of life-5dimension5-levels

    European Quality of life-5dimension5-levels is descriptive system that measures patients health related quality of life. This system consists of 5 dimensions: Mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension consists of 5 levels: no problems, slight problems, moderate problems, severe problems, and extreme problems.

    Measured: At baseline, and month 12, 24, 36, 48, and 60.

  13. Duration and cumulative glucocorticoid dosage

    It is known that treatment with glucocorticoid dosage in patients with inflammatory diseases is the number one reason for drug-induced hyperglycaemia and DM, and that GC can aggreviate hyperglycaemia in patients with a prior diagnosis of DM.

    Measured: At baseline, and month 1, 3, 6, 12, 24 and 36.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Aug 2023
  2. Study start1 Aug 2023
  3. Primary completion1 Sep 2025
  4. Study completion1 Sep 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
198 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06011512
Sponsor's protocol ID
AalborgGCA
Status last verified
Apr 2026
First submitted
10 Aug 2023
Last updated
30 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Giant Cell Arteritis and Polymyalgia Rheumatica, run by Salome Kristensen at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proportion of participants developing diabetes mellitus during the study period, measured in changes of HbA1c. (time frame: At baseline, and month 1, 3, 6, 12, 24 and 36.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Apr 2026.

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