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NCT06382753 Clinical Trial

Impact of Periodontal Supportive Therapy in Patients With Gingivitis and Periodontitis

Periodontitis Clinical Trial

Official title:
Impact of Periodontal Supportive Therapy Number of Sessions in Patients With Gingivitis and Periodontitis in Order to Evaluate Disease Evolution.

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06382753
Other study ID # 20-24-PAR
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 20, 2024
Est. completion date June 30, 2024

Study information
Verified date April 2024
Source University of Catania
Contact Gaetano Isola
Phone 0953785652
Email gaetano.isola@unict.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study evaluated the number of sessions of periodontal supportive treatment in patients with gingivitis in order to evaluate the risk of periodontitis development.

Description:

Patient with gingivitis were retrospectively evaluated. The number of periodontal supportive therapy were recorded other than gingivitis periodontal parameters over 5-years follow-up.

Recruitment information / eligibility
Status Recruiting
Enrollment 150
Est. completion date June 30, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Diagnosis of Gingivitis Exclusion Criteria: - Diagnosis of Periodontitis - Pregnancy - Systemic diseases

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Gingival inflammation
Patients were scored for their status of gingival inflammation using Gingival Index and Bleeding on Probing Scores

Locations
Country Name City State
Italy AOU Policlinico G. Rodolico Catania

Sponsors (1)
Lead Sponsor Collaborator
University of Catania

Country where clinical trial is conducted

Italy, 

Outcome
Type Measure Description Time frame Safety issue
Primary Bleeding on Probing Evaluation of bleeding on probing reduction 5-years
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