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Haemochromatosis and Periodontitis

Haemochromatosis and Periodontitis

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04006249
Acronym
HEMOPARO
Enrollment
87
Registered
2019-07-05
Start date
2010-06-06
Completion date
2011-12-01
Last updated
2026-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemochromatosis

Brief summary

Periodontitis is a chronic inflammatory disease that affects tissues surrounding the teeth. It is strongly associated with the major pathogenic "red complex", including Porphyromonas gingivalis, Tannerella forsythia and Treponema denticola1 and thus is considered an infection. Recent advances in the pathogenesis of periodontal disease have suggested that polymicrobial synergy and microbiota dysbiosis together with a dysregulated immune response can induce inflammation-mediated damage in periodontal tissues2-4. Interestingly, currently periodontitis is associated with a growing number of systemic diseases, including cardiovascular diseases, adverse pregnancy outcomes, diabetes5-7 and hereditary haemochromatosis8.

Interventions

DIAGNOSTIC_TESTdental probes

Measurement of the depth of the periodontal pockets and clinical loss

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
35 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 35 to 64 years with homozygosity hemochromatosis C282Y * Patients regularly enrolled in a health insurance plan * Patients with at least 10 natural teeth * Patients who have given informed written, dated and signed consent

Exclusion criteria

* Diabetic patients * Simultaneous participation in another study * Pregnant or lactating women * The incapacitated persons and persons deprived of their liberty * Patients who do not speak French, both written and spoken * Patients previously included in this trial * Patients with heart valves or endovascular equipment (risk of infective endocarditis ...) * Patients with a history of maxillofacial surgery * Patients whose oral status is considered incompatible with entry into the study, at the discretion of the investigator * Patients on drugs that can cause gingival hypertrophy, such as Hydantoins (phenytoin), Dihydropyridines, Diltiazem or Ciclosporin * Patients on medication that can cause gingival bleeding (anticoagulants, antiplatelet agents and aspirin).

Design outcomes

Primary

MeasureTime frameDescription
prevalence of periodontal diseases2 yearsTo evaluate the prevalence of periodontal diseases in patients with hemochromatosis at the time of diagnosis and / or their usual therapeutic

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026