Phase
Condition
Down's Syndrome
Inflammation
Periodontitis
Treatment
Inclusion visit (J0)
Screening visit (J-21)
Biological sampling
Clinical Study ID
Ages 3-12 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Common to all groups:
Age: 3 to 12
Patient affiliated to a social security program, beneficiary not covered by the AME.
Legal representatives who speak and understand French well enough to be able to readand understand the study information.
Legal representatives giving written consent for their child's participation in thestudy.
Specific:
Case Group:
Trisomy 21 patient with gingival inflammation (subgroup 1)
Trisomy 21 patient with healthy gingiva on intact periodontium with no history ofperiodontitis (subgroup 2)
Control Group: child meeting one of these criteria:
Patient with psychomotor retardation with no known repercussions on the orofacialsphere or immunity, presenting gingival inflammation (subgroup 1)
Patients with psychomotor retardation and no known repercussions on orofacial healthor immunity, presenting gingival health on intact periodontium with no history ofgingival inflammation (subgroup 2).
Patients with no known general pathology and gingival inflammation (subgroup 3)
Patients with no known general pathology and healthy gingiva on intact periodontiumwith no history of gingival inflammation (subgroup 4)
Exclusion
Exclusion Criteria:
Common to all groups:
Patient having received antibiotic prophylaxis, antibiotic therapy oranti-inflammatory treatment in the 3 months prior to inclusion
Patient included in another interventional research protocol or in a period ofexclusion.
Patient on AME
Patients with a contraindication to the use of MEOPA:
Patients requiring pure oxygen ventilation
Intracranial hypertension
Unevaluated head trauma
New-onset, unexplained neurological abnormalities
Pneumothorax
Emphysema bubbles
Gas embolism
Diving accident
Abdominal gas distension, occlusion
Patient recently treated with ophthalmic gas (SF6, C3F8, C2F6)
Known, unsubstituted vitamin B12 deficiency
Specific to Trisomy 21 group:
- Patient with no genetic diagnosis
Study Design
Study Description
Connect with a study center
Carles-Foix Hospital
Ivry-sur-Seine, 94200
FranceActive - Recruiting
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