Chronic Periodontitis
Conditions
Interventions
Sponsors
Tobita Morikuni
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Have a Periodontal pocket more than 5 mm at baseline examination. 2) Intrabony defect is 5 mm and more depth, and 2 mm and more width at interproximal site of the experimental tooth by X-ray examination. 3) Already have received initial preparation at the screening. 4) Hized gingiva and for whom flap surgery is deemed appropriate. 5) Persons whose oral hygiene is established Good oral hygiene. 6) 18 years and older. 7) Signed informed consent 8) The principal investigator believes makes him/her suitable for participation in this clinical study.
Exclusion criteria
Exclusion criteria: 1) Can not be measured clinical attachment level of experimental tooth. 2) Have a history of Complicate malignant tumor. 3) Suspected of oral malignant tumor or precancerous lesion. 4) Need to undergo the treatment, such as surgical treatment, restorative treatment or root canal treatment, at the experimental tooth within 36 weeks after transplant. 5) Pregnancy, during breastfeeding, or possibility of pregnancy. 6) Persons who suffer from disorders of kidney, liver or blood 7) Have disease of kidney, liver and/or blood. 8) Have active infectious diseases. 9) Alcoholism or Drug dependence. 10) Mental or consciousness disorder. 11) HCV antibody, HBs antigen, ATLA virus antibody or HIV antibody positive person. 12) Smoke more than 10 pieces per day. 13) Have anti-coagulant or anti-platelet medications, or have a bleeding disorders. 14) Other,the investigator believes makes him/her unsuitable for participation in the clinical study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety | — |
Secondary
| Measure | Time frame |
|---|---|
| Efficacy | — |
Countries
Japan
Contacts
Public ContactMika Iguchi
Juntendo university
Outcome results
None listed