Clinical evaluation of GrandioSO Heavy Flow in combination with the restorative material GrandioSO for Class I and II restorations

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00033585

Enrollment

Registered

2024-04-29

Start date

2011-08-22

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

K02.9

Interventions

Group 1: Control group (restaurtion using composite material without an addional layer of flowable composite) Group 2: Test group (restaurtion using composite material in combination with an addional

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: signed consent form available positive vitality teeth needing indirect pulp capping 2 molars/premolars with Class I/II cavity lesions with: - antagonist - approximal contact - bucco-oral extension at least one third of the spacing of tooth cusps

Exclusion criteria

Exclusion criteria: severe systemic diseases allergies related to materials pregnancy or breastfeeding inadequate oral hygiene preoperative pulpal symptoms teeth needing direct pulp capping endodontically treated teeth

Design outcomes

Primary

Measure	Time frame
48 months	—

Secondary

Measure	Time frame
36 months	—

Countries

Germany

Contacts

Public ContactChristian Gernhardt

Martin-Luther-Universität Halle-Wittenberg, Universitätspoliklinik für Zahnerhaltungskunde und Parodontologie

christian.Gernhardt@uk-halle.de03455573741

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026