None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Subjects of either sex between the age group of 18-60 years, who sign informed consent for the study. 2.Systemically healthy subjects 3.Subjects with Periodontitis having probing pocket depth of greater than or equal to 6mm and clinical attachment level of greater than or equal to 6mm after phase I therapy in at least one tooth. 4.At least one site that radiographically shows vertical bone loss greater than or equal to 4 mm 5.Subjects having minimum of one maxillary or mandibular tooth indicated for extraction [non root canal treated tooth] Non-smokers.
Exclusion criteria
Exclusion criteria: 1.Pregnant women or expected pregnancy during the study period. 2.Lactating women. 3.Presence of uncontrolled metabolic, endocrine, blood, neoplastic, or renal diseases. 4.History of Alcoholism or drug abuse. 5.Patients on any medication which is known to interfere with bone remodelling. 6.Any other conditions that might interfere with the analysis of the results.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Radiographic Changes in the bone defect area BDA ( in mm2) Any adverse reaction of Autologous Tooth Dentin graftsTimepoint: will be measured at baseline & after 6 months | — |
Primary
| Measure | Time frame |
|---|---|
| Changes in probing depth (PD) in the defect site . Changes in clinical attachment level CAL in the defect siteTimepoint: At Baseline , at One month , at Six month | — |
Countries
India
Contacts
maulana azad institute of dental sciences