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Periodontitis, AdultDENT-PCNCT07688278

HbA1c Screening in Dental Care and Primary Care Referral in Patients With Advanced Periodontitis

A study testing Point-of-care HbA1c screening and Conditional standardized primary care referral in people with Periodontitis, Adult and Prediabetes / Type 2 Diabetes, run by Region Skane at 1 site in Sweden.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

This study will evaluate whether HbA1c screening can be performed in dental care to detect elevated blood glucose in patients with advanced periodontitis and support referral to primary care. Periodontitis is a common chronic inflammatory disease affecting the supporting tissues of the teeth. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Point-of-care HbA1c screening and Conditional standardized primary care referral
Could I receive a placebo?
No, everyone receives an active treatment
How many people
600 participants
Where
1 siteSweden
Study dates
1 Jul 2026to 31 Dec 2027
Phase
Interventional

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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18 years or older.
  • Advanced periodontitis, defined as stage 3-4 periodontitis or grade B/C periodontitis according to clinical and radiographic assessment during routine dental care.
  • Ability to understand study information and provide informed consent.

Who cannot join

  • Previously diagnosed diabetes mellitus.
  • Inability to provide informed consent, for example due to severe mental disorder or markedly impaired health status as judged by the clinical staff.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Peter Nymberg contact

peter.nymberg@med.lu.se

Sweden1 site, 1 recruiting
  • Folktandvården Skåne AB

    Skåne

    Nils Oscarson, +46 70 277 33 57, nils.oscarson@folktandvardenskane.se

    Nils Oscarson

    Recruiting

Other trials in Sweden

About this study

Official title: Early Detection of Elevated Blood Sugar in Patients With Advanced Periodontitis: a Feasibility Study

This study will evaluate whether HbA1c screening can be performed in dental care to detect elevated blood glucose in patients with advanced periodontitis and support referral to primary care.

Periodontitis is a common chronic inflammatory disease affecting the supporting tissues of the teeth. Advanced periodontitis is associated with prediabetes, type 2 diabetes and cardiovascular disease. The relationship between periodontitis and diabetes is bidirectional: diabetes increases the risk and severity of periodontitis, while periodontal inflammation may contribute to impaired glucose regulation. Patients with advanced periodontitis may therefore represent a group at increased risk of undetected elevated blood glucose. Many of these patients visit dental care regularly but may not otherwise be reached by structured medical prevention.

Read more

This is a cross-sectional observational feasibility study conducted in public dental clinics in Skåne, Sweden, in collaboration with primary care. Adult patients aged 18 years or older with advanced periodontitis, defined as periodontitis stage 3-4 or grade B/C, will be invited to participate during a routine dental visit. Patients with previously diagnosed diabetes will not be included.

After informed consent, participants will complete or update a health declaration and undergo capillary HbA1c testing at the dental clinic using a validated point-of-care instrument. Participants will receive their test result. Those with HbA1c ≥42 mmol/mol will receive standardized information and be referred to their listed primary care centre for further diagnostic assessment and preventive follow-up according to routine clinical practice.

The study will assess how feasible this pathway is in routine dental care. Outcomes include participation rate, successful HbA1c testing, time required for study procedures, prevalence of elevated HbA1c, proportion referred to primary care, completed primary care follow-up within six months, dropout and costs. Follow-up data will be collected from medical records and regional registers.

The study may provide a practical model for collaboration between dental care and primary care, with the long-term aim of improving early detection of prediabetes and diabetes and strengthening preventive care for patients with advanced periodontitis.

Being tested
Point-of-care HbA1c screening, Conditional standardized primary care referral
Medical subject headings
Chronic Periodontitis, Prediabetic State, Diabetes Mellitus, Type 2

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Point-of-care HbA1c screeningDiagnostic test

    All participants undergo capillary HbA1c testing at the dental clinic using a validated point-of-care instrument. Test results are provided to the participant during the visit.

  • Conditional standardized primary care referralOther

    Participants with HbA1c ≥42 mmol/mol receive standardized information about the elevated test result and are referred to their listed primary care centre for further diagnostic assessment and preventive follow-up according to routine clinical practice.

Study groups in NCT07688278
Study groupRoleWhat they receive
HbA1c Screening in Dental CareExperimentalAdult patients with advanced periodontitis undergo point-of-care HbA1c screening during a routine dental care visit. Patients with HbA1c ≥42 mmol/mol receive standardized information and are referred to primary care for further assessment and preventive follow-up.
Receives: Diagnostic Test: Point-of-care HbA1c screening; Other: Conditional standardized primary care referral

What is being measured

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

  1. Participation rate

    Number of participants included out of those who meet the inclusion criteria. Reasons for non-participation will be recorded in free text.

    Measured: 6 months

Secondary outcomes (5)
  1. Proportion of participants with HbA1c 42 mmol/mol or higher.

    Proportion of participants with HbA1c 42 mmol/mol or higher

    Measured: 6 months

  2. Proportion of patients undergoing blood pressure examination at follow-up in primary care

    Through review of medical records at the patient's primary health care center, assessment of proportion of patients undergoing blood pressure examination.

    Measured: 6 months

  3. Proportion of patients undergoing blood lipid laboratory samples

    Through review of medical records in primary care, assessment of proportion of patients undergoing blood lipid laboratory sample.

    Measured: 6 months

  4. Diagnosis at follow-up

    Diagnosis registered at the follow-up in primary care

    Measured: 6 months

  5. Proportion of patients receiving lifestyle advice at follow-up

    Through review of medical records at follow-up in primary care, assessment of proportion of patients receiving advice on lifestyle habits.

    Measured: 6 months

Timeline

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

  1. First posted7 Jul 2026
  2. Study start1 Jul 2026 (estimated)
  3. Primary completion30 Jul 2027 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
600 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07688278
Sponsor's protocol ID
2025-01744-01
Other IDs
2025
Acronym
DENT-PC
Status last verified
May 2026
First submitted
29 May 2026
Last updated
7 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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