JPRN-jRCTs032190123
Completed
Phase 1
Efficacy of maxillary sinus augmentation using long-term absorbable GBR membrane(GMEM-B2)
MUNAKATA MOTOHIRO0 sites25 target enrollmentOctober 28, 2019
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- MUNAKATA MOTOHIRO
- Enrollment
- 25
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.20 years old or older and less than 65 years old
- •2\.Non\-smoker
- •3\.Patients with bone mass less than 4 mm planned implant placement site according to CT examination results
- •4\.Patients obtained written informed consent about participation in this study
Exclusion Criteria
- •1\.Removable prosthetics
- •2\.Patient with respiratory disease
- •3\.Osteoporosis, severe diabetes, rheumatoid arthritis, bone metabolism diseases such as taking steroids or BP drugs and those taking medications
- •4\.Patients with alcohol and drug addiction, mental illness
- •5\.Patients with cyst or tumor / inflammation in maxillary sinus on CT examination result
- •6\.Patients who had got the radiation therapy.
- •7\.Patients with heart disease, blood disease, collagen disease
- •8\.Patients with kidney failure or dialysis
- •9\.Patients who are pregnant and lactation period
- •10\.Patients with a history of hypersensitivity or allergy to copolymer of e\-caprolactone and L\-lactide
Outcomes
Primary Outcomes
Not specified
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