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Clinical trial for masking of dental fluorosis by infiltration

Clinical trial for masking of dental fluorosis by infiltration - FIT-Research Study 2016 (Fluorose-Infilrtation-Technique)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00010465
Enrollment
40
Registered
2016-08-26
Start date
2017-02-07
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

K00.3 K03.6

Interventions

Group 1: Group 1 (Placebo Bleaching therapy + Infiltration therapy) Masking of the dental fluorosis with ICON infiltration (DMG, Hamburg) after previous placebo bleaching therapy of the teeth 15-25 a
Rotterdam, Netherlands). Group 2: Group 2 (Bleaching therapy + Infiltration therapy) Masking of the dental fluorosis with ICON infiltration (DMG, Hamburg) after previous In-Office-Bleaching of the t
Rotterdam, Netherlands).

Sponsors

Zentrum für Zahn-, Mund- und Kieferheilkunde Poliklinik für Zahnerhaltung und Parodontologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: • Light to moderate fluorotic lesions during mineralisation of the teeth 15 to 25 and 35 to 45 (TF Index = 1-5) • Male and female patients of 18+ years at the time of recruitment • Legal competence • A written informed consent of the subject/patient to apply to the study voluntarily is mandatory

Exclusion criteria

Exclusion criteria: • Attendance to other interventional examinations • Contraindications in accordance with prescribing information or package information • Allergies towards one of the contents or contact allergies • Severe general diseases (ASA > 1) • Previous restorative treatment of the fluorotic enamel areas of the teeth 15-25 and 35-45 • Bleaching of the teeth 15-25 and 35-45 within the last 18 months [Auschill TM, Schneider-Del Savio T, Hellwig E, Arweiler NB 2012] • Evidence of the participating person presumably not following the study protocol (e.g. lack of cooperativeness) • Accommodation in an institution due to court injunction or official arrangement

Design outcomes

Primary

MeasureTime frame
• Reduction of the color difference ?E between fluorotic lesions and healthy enamel immediately after treatment (1 hour after completion of infiltration) in comparison to the initial situation (difference). The treatment results are evaluated photo-optically with standardized photographs and subsequent digital photo analysis (ImageJ). For photo-optical analysis an index tooth is determined. The index tooth shows the most servere dental fluorosis. By using the formula ?E = ((?L*)2+(?a*)2+(?b*)2)1/2 , the color difference can be calculated.

Secondary

MeasureTime frame
•Reduction of the color difference ?E below the limit of a normal conversation distance visible to the human eye according to ?E = 3.7 [Johnston and Kao 1989] (1 hour after completion of infiltration) •Patient satisfaction (PZ) + OHIP 14 according to the overall aesthetic result and the treatment comfort (1 hour after completion of infiltration) •Long-term results; Improvements after treatment during the observation period (1, 3, 6 months) (variables: ?E and optical assessment by non-specialist judge; PZ) •Accordance of the colorimeter VITA Easyshade V's ?E value and the standardized, digital photographs evaluated by ImageJ

Countries

Germany

Contacts

Public ContactChristoph Schoppmeier

Zentrum für Zahn-, Mund- und Kieferheilkunde Poliklinik für Zahnerhaltung und Parodontologie

christoph.schoppmeier@uk-koeln.de00492214784736

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 5, 2026