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Tooth shape corrections and tooth widenings with directly applied composite materials-an application observation

Tooth shape corrections and tooth widenings with directly applied composite materials-an application observation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00013582
Enrollment
250
Registered
2018-01-03
Start date
2018-02-22
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

Overall survival of direct composite buildups and tooth widening restorations

Interventions

Group 1: Follow-up examination 5-15 years after tooth shape corrections and tooth widenings with directly applied composite materials: For evaluation a routine dental check will be carried out as fol

Sponsors

Universitätsklinikum Heidelberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patient has received a form correction or tooth widening with directly applied composite materials between 01/2001 and 12/2012 in the Department of Dentistry Conservation of the Clinic for Oral, Dental and Jaw Diseases of the University Hospital of Heidelberg Patient has received a form correction or tooth widening with directly introduced composite materials between 01/2001 and 12/2012 in the Polyclinic for Tooth Preservation and Periodontics of the Clinic for Oral, Dental and Maxillofacial Diseases of the University Hospital Würzburg Patient is healthy Patient is able to consent

Exclusion criteria

Exclusion criteria: Physical limitations or disabilities that do not allow the patient normal oral hygiene Signs of heavily neglected oral hygiene (severe periodontal disease or rapidly progressing tooth decay) Patient is pregnant or breastfeeding Illness of the patient requiring medical shielding from dental treatment Current or ongoing participation in another clinical trial during the last 30 days

Design outcomes

Primary

MeasureTime frame
Survival of restorations between 5 and 15 years of clinical service „Overall Survival“ – Restauration ist completely intact at time of evaluation „Functional Survival“ – Restauration is in situ at time of evaluation a) during the observation period unfavourable events occured that made an intervention (repair of restoration) necessary b) durng observation unfavourable an event is recorded „Failure“ – complete loss of restoration during follow up

Secondary

MeasureTime frame
Clinical Quality Criteria between 5 and 15 years of clinical Service: At time of evaluation the quality outcome of each restoration will be scored by the modified USPHS/FDI-criteria

Countries

Germany

Contacts

Public ContactCornelia Frese

Universitätsklinikum Heidelberg Poliklinik für Zahnerhaltungskunde

cornelia.frese@med.uni-heidelberg.de06221 5639886

Outcome results

None listed

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