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Influence of post-procedural polishing after GBT on discoloration, tooth sensitivity and patient satisfaction

Influence of post-procedural polishing after GBT on discoloration, tooth sensitivity and patient satisfaction - Influence of post-procedural polishing after GBT

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00025351
Enrollment
40
Registered
2023-06-28
Start date
2022-09-30
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

Air-Polishing with or without rubber cup /polishing paste application

Interventions

Group 1: Periodontal healthy patients willing to participate in this study will be treated at their biannual dental hygiene appointment for split-mouth biofilm removal, with one side of the dentition

Sponsors

Universität Zürich, Zentrum für Zahnmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Compliant patients =18 years of age, who attend their regular recalls and are well-instructed to their regular individual oral hygiene instruments in our clinic for at least 2 years. - Patients must be systemically healthy. - Group A: Periodontally healthy patients (PSI 0-2) without attachment loss and no pockets exceeding 4 mm - Group B: Periodontally stable patients (PSI 0-3) with attachment loss but no pockets exceeding 4 mm

Exclusion criteria

Exclusion criteria: - Poor oral hygiene and compliance - Active periodontal disease with pockets > 4 mm - History of radiation in head-neck area - Systemic or local disease or condition that can compromise saliva composition and flow (including Reflux) - Use of drugs influencing saliva composition and flow - Pregnancy - Poor compliance or unwillingness to return for follow-ups

Design outcomes

Primary

MeasureTime frame
Discoloration after airpolishing with and without rubber cup/polishing paste usage, evaluated at 4, 12 and 24 weeks (end-point is the standard recall time for periodontally healthy patients).

Secondary

MeasureTime frame
1. Tooth hypersensitivity changes from baseline to bi-yearly recall, measured at 4, 12 and 24 weeks 2. Patient satisfaction

Countries

Switzerland

Contacts

Public ContactPatrick R. Schmidlin

Universität ZürichZentrum für Zahnmedizin

patrick.schmidlin@zzm.uzh.ch+41 44 634 34 17

Outcome results

None listed

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