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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05558293
Other study ID # 20-2018-10
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2022
Est. completion date December 5, 2022

Study information

Verified date November 2023
Source University of Catania
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In light of the controversy that are already approved but that however still exists regarding the efficacy and influence of the protocols for the management of periodontitis, the aim of this study was to evaluate, at 6 months follow-up, the post-treatment clinical parameters and immunological and gingival microbial profiles in patients with periodontitis, treated by either SRP in addition to full mouth periodontal debridement.


Description:

This trial was conducted in accordance with the World Medical Association's Declaration of Helsinki of 1975, and reviewed in 2008. Patients were enrolled from January 2020 to December 2022. The local ethical committee of approved the study protocol (125/PO) and each patient was carefully informed about the possible inherent risks of the study and provided their informed written consent 88 patients, aged 27 to 65 (mean age 57) were assessed for eligibility. In all subjects, subgingival plaque will acquired from 4 separate proximal periodontal sites.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date December 5, 2022
Est. primary completion date December 5, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 65 Years
Eligibility Inclusion Criteria: 1. good condition of general health, 2. a minimum of 2 teeth for each quadrant with a Pocket Depth (PD) ranging from 4-6 mm, 3. no involvement of the furcation, 4. a minimum of a six teeth per quadrant, respectively. Exclusion Criteria: 1. periodontal therapy during the last 12 months, 2. assumption of antibiotics during the last 6 months, 3. pregnancy, 4. any systemic condition which might affect the effects of the study treatment, 5. previous or current radiation or immunosuppressive therapies, 6. use of mouthwash containing antimicrobials during the previous 3 months, 7. no use of hormonal contraceptives, 8. medication by anti-inflammatory and immunosuppressive drugs, 9. previous history of hard-drinking, 10. smoking, 11. class II and III tooth mobility.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Scaling and root planing
Full mouth or quadrant SRP

Locations

Country Name City State
Italy University of Catania Catania CT

Sponsors (1)

Lead Sponsor Collaborator
University of Catania

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Probing depth changes Measurment of Probing Depth changes in millimeters 6 months
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