Evaluation of performance and satisfaction of complete dentures fabricated by digital and conventional methods
- Conditions
- Diseases of the digestive system
- Registration Number
- KCT0005692
- Lead Sponsor
- Yonsei University Health System, Dental Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 13
· 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
· 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
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method denture adaptation
- Secondary Outcome Measures
Name Time Method masticatory force;masticatory efficiency;satisfaction