Clinical feasibility study for periodontal diagnostics using intraoral scanners

Recruiting

• Conditions: K05; Gingivitis and periodontal diseases

• Registration Number: DRKS00017662
• Lead Sponsor: Poliklinik für Zahnerhaltungskunde, Universitätsklinikum Heidelberg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-09-09
• Results First Posted: 2023-12-19
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

Diagnosis: Periodontitis or condition after periodontitis therapy

Exclusion Criteria

Limited ability to consent, less than 12 teeth present

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome parameters of the examination are the periodontal probing depths and attachment level loss over a period of 18 months, as well as volume changes in the gingival area of natural teeth and dental implants when comparing digital impressions over time.

Secondary Outcome Measures

Name	Time	Method
Secondary outcome parameters are volume changes of the gingiva during active periodontitis therapy, patient comfort, all findings of the clinical dental examination (number of teeth, restorations and dental prostheses, bleeding or pus on probing, clinically visible signs of inflammation) and duration of intraoral images.