Comparison of two self-adhering sealants after 12 months - in-vivo

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00015854

Enrollment

Registered

2018-11-26

Start date

2014-06-17

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

K02.0 K02.1

Interventions

Group 1: Sealant with Beautisealant Group 2: Sealant with VertiseFlow

Eligibility

Sex/Gender

All

Age

6 Years to 14 Years

Inclusion criteria

Inclusion criteria: Examination tooth: pierced and caries-free 1st / 2nd molar Caries free according to ICDAS II, code 0 Submission of the consent form Permanent tooth (2nd dentition)

Exclusion criteria

Exclusion criteria: severe general diseases, carious lesion on the examination tooth, Patients with clearly restricted mouth opening, lack of cooperation, serious oral diseases, known hypersensitivity to a substance used in the study, unsigned declaration of consent, gingivitis, Draining the tooth is not possible

Design outcomes

Primary

Measure	Time frame
Assessment of the quality of fissure seals after 12 months - in vivo. The target criterion was retention of two pit- and fissure sealants. For this purpose, the teeth were photographed before and after the seal and reevaluated after 12 months. Sealer losses were compared to the input shots and recorded. The retention rate was divided into complete, minor loss, loss up to half and loss over half.	—

Secondary

Measure	Time frame
Other parameters were: Peripheral analysis after staining, incidence of caries, aesthetics, postoperative sensitivity. Patient satisfaction with the seal.	—

Countries

Germany

Contacts

Public ContactChristopher Baartz

Zahnarztpraxis

Praxis-Baartz-Thiemann@web.de025997272

Outcome results

None listed

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