None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Healthy men and women over 20 years of age 2. Patients who are needed of least one or more tooth extractions in the maxillary or mandible 3. Patients who can respond in good faith on a regular recall until termination of clinical trial 4. Patients who fully understand the details of the trial and obtain a written consent
Exclusion criteria
Exclusion criteria: 1. Patients with uncontrolled hypertension or diabetes 2. Patients with a history of malignancy or current diseases in the jaw 3. Patients with complications of serious cardiovascular disease, respiratory disease, heart disease, liver disease, digestive disorders, blood system diseases and neurological disorders•psychiatric disorders 4. Patients with hyperthyroidism or hypothyroidism 5. Patients with a history of drug allergy 6. Patients who have depression or anxiety disorder, and will influence the evaluation of efficacy 7. Patients with history of drug or alcohol abuse within a year or current abuse 8. Unlikely to be able to comply with study procedures according to Investigators judgement 9. Patients with allergic or hypersensitivity reactions to implant, bone graft material and barrier membrane
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Absorption rate of implanted bone graft material using a Cone-beam CT;Volume measurements of hard and soft tissue around alveolar ridge using a Cone-beam CT;Adverse and inflammatory reactions | — |
Secondary
| Measure | Time frame |
|---|---|
| Ease of handling ; VAS (Visual Analogue Scale) | — |
Countries
Korea, Republic of
Contacts
Yonsei University