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Influence of the number of implants in the edentulous mandible on chewing efficiency - a clinical study within subject design

Influence of the number of implants in the edentulous mandible on chewing efficiency - a clinical study within subject design

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00011087
Enrollment
13
Registered
2016-11-14
Start date
2016-05-20
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

edentulism

Interventions

Group 1: All patients will receive three implants in the edentulous mandible, which are loaded at different times. After two months of submerged healing, the first implant will be connected to the den

Sponsors

Universitätsklinikum Schleswig-Holstein Campus Kiel
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: edentulous maxilla and mandible with no contraindication for implant placement. technically acceptable complete dentures in mandible and maxilla. A patient who feels there is adequate retention and stability in current maxillary denture but is unsatisfied with the retention and/or stability of the current mandibular denture. Current dentures have been worn for at least three months to allow for adaptation.

Exclusion criteria

Exclusion criteria: Contraindication for implant placement, Technically insufficient dentures, Residual teeth or implants in the maxilla or mandible

Design outcomes

Primary

MeasureTime frame
Enhancement of the chewing efficiency, measured by the objective masticatory performance three months after loading of a different number of implants.

Secondary

MeasureTime frame
Oral Health related quality of life is measured by a questionnaire three months after loading each additional implant. Patients’ denture satisfaction is measured by a VAS questionnaire three months after loading each additional implant. Prothetic complications will be documented continuously throughout the clinical trial.

Countries

Germany

Contacts

Public ContactNicole Passia

Klinik für Zahnärztliche Prothetik, Propädeutik und WerkstoffkundeUniversitätsklinikum Schleswig-Holstein, Campus Kiel

npassia@proth.uni-kiel.de0049-431-500-26402

Outcome results

None listed

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