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Bioavailability of fluoride in saliva after administration of fluoridated bioactive glass.

Bioavailability of fluoride in saliva after administration of fluoridated bioactive glass. - Fluoridated bioactive glass

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00016038
Enrollment
48
Registered
2018-12-05
Start date
2018-03-05
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

Z29

Interventions

Group 1: Test subjects are brushing their teeth with a toothpaste containing 1450 ppm NaF (Eurodont, MAXIM Markenprodukte, Pulheim, Germany). Toothbrushing is carried out according to the Bass method
BIOMIN, London, UK).

Sponsors

Universität Witten/Herdecke Professur für biologische und materialkundliche Grundlagen der Zahnmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 28 Years

Inclusion criteria

Inclusion criteria: Caries free, good oral health, normal saliva secretion

Exclusion criteria

Exclusion criteria: Systemic diseases, periodontitis, other oral diseases

Design outcomes

Primary

MeasureTime frame
Primary endpoint is the comparison of the fluoride concentration in saliva application of NaF, AmF and fluoridated bioactive glas at measuring points T3 and T4. The null hypothesis is that there are no differences between the applied fluoride formulations Secondary endpoint is the comparison of the fluoride concentration within the groups (NaF, MaF and fluoridated bioactive glass) at the measuring points T1, T2, T3 and T4 compared to T0

Secondary

MeasureTime frame
Comparison of the different measuring time points

Countries

Germany

Contacts

Public ContactElla Naumova

Universität Witten/Herdecke Professur für biologische und materialkundliche Grundlagen der Zahnmedizin

ella.naumova@uni-wh.de02302926640

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 2, 2026