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Clinical feasibility study for periodontal diagnostics using intraoral scanners

Clinical feasibility study for periodontal diagnostics using intraoral scanners

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00017662
Enrollment
200
Registered
2019-09-09
Start date
2020-01-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

K05

Interventions

Group 1: In patients undergoing supportive periodontal therapy, virtual impressions are taken over an observation period of 18 months during each session. Group 2: In patients who have not previously

Sponsors

Poliklinik für Zahnerhaltungskunde, Universitätsklinikum Heidelberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Diagnosis: Periodontitis or condition after periodontitis therapy

Exclusion criteria

Exclusion criteria: Limited ability to consent, less than 12 teeth present

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Germany

Contacts

Public ContactSarah Kristin Sonnenschein

Poliklinik für Zahnerhaltungskunde, Universitätsklinikum Heidelberg

sarah.sonnenschein@med.uni-heidelberg.de06221-56-6002

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026