None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: · Subjects aged 20 years or older · Subjects with full edentulism or those who will transition to fully edentulous state after extraction of all residual teeth · Subjects who voluntarily decided to participate in the study, having given written informed consent prior to undertaking any study-related procedure
Exclusion criteria
Exclusion criteria: · Subjects who cannot read the informed consent form · Subjects having problem with mouth opening and closing due to temporomandibular disorders · Subjects with congenital or acquired defects in the maxilla and/or mandible · Subjects judged to be inappropriate by the principal investigator or contact person due to clinically significant medical or psychiatric findings · Subjects whose participation is inappropriate as judged by the principal investigator because of ethical reason or because their participation may affect the results of the clinical trial
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| masticatory force;masticatory efficiency;satisfaction | — |
Primary
| Measure | Time frame |
|---|---|
| denture adaptation | — |
Countries
Korea, Republic of
Contacts
Yonsei University Health System, Dental Hospital