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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01246596
Other study ID # 10-AOI-01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2011
Est. completion date May 5, 2014

Study information

Verified date November 2023
Source Centre Hospitalier Universitaire de Nice
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The etiopathogenesis of periodontal disease results from complex interaction between infectious agents, mainly including bacteria, and host cellular and humoral immune responses. However it is thought that bacteria-induced pathogenesis is not sufficient alone to explain all biological and clinical features of the destructive periodontal disease. The main hypothesis is that herpesviruses, such as Epstein-Barr Virus, may participate as well by altering epithelial gingival cell biology and consequently may promote the initiation and progression of periodontitis.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date May 5, 2014
Est. primary completion date May 5, 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 10 patients affected by chronic periodontitis - 10 patients affected by aggressive periodontitis - 10 healthy patients (orthodontics extraction) - Subject who have read and understood the information note relative under investigation and who have signed the informed consent - major patient Exclusion Criteria: - Patient with no contre-indication to periodontal treatment - Patient with serious blood disease - Patient who exhibits systemic condition incompatible with realization of the study - Patient treated with oral retinoids, bisphosphonates, oral anticoagulants and anticonvulsivants - Patient who presents a buccal carcinoma treated with radiotherapy - Patient who have received during the past 6 months: anti-inflammatory drugs, anti-cancerous or immunosuppressive chemiotherapy - Patient who presents a linguistic or psychic incapacity to understand information

Study Design


Intervention

Procedure:
dental root planing
The objective of root planing, otherwise known as conventional periodontal therapy, non-surgical periodontal therapy, or dental prophylaxis is to remove or eliminate the etiologic agents which cause inflammation: dental plaque, its products and calculus,[1] thus helping to establish a periodontium that is free of disease.[2]
dental root planing
The objective of root planing, otherwise known as conventional periodontal therapy, non-surgical periodontal therapy, or dental prophylaxis is to remove or eliminate the etiologic agents which cause inflammation: dental plaque, its products and calculus, thus helping to establish a periodontium that is free of disease.
dental root planing
The objective of root planing, otherwise known as conventional periodontal therapy, non-surgical periodontal therapy, or dental prophylaxis is to remove or eliminate the etiologic agents which cause inflammation: dental plaque, its products and calculus, thus helping to establish a periodontium that is free of disease.

Locations

Country Name City State
France Dr Severine VINCENT Nice

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of gingival epithelial cells infected by EBV (by immunofluorescence and In situ Hybridization) at time=0
Secondary Epithelial tissue infected by EBV (by immunofluorescence and in situ hybridization) at time = 0
Secondary Presence / absence of latency and / or lytic proteins (by immunofluorescence and in situ hybridization) at time = 0
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