Actively Recruiting
Alveolar Ridge Preservation After Tooth Extraction Using Autologous Dentin Matrix
Led by Moscow State University of Medicine and Dentistry · Updated on 2024-08-07
80
Participants Needed
1
Research Sites
261 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
According to the scientific literature, the loss of any tooth can be accompanied by a pronounced resorption of the alveolar ridge in the corresponding area, which leads to the formation of various defects. In the post-extraction period, bone tissue resorption 4 months after tooth extraction is up to 45% horizontally and 43% vertically.Despite the considerable amount of research on this problem, the improvement of pre-implantation preparation of patients with adentia after tooth extraction continues to be an extremely urgent task. The solution to this problem requires a comprehensive approach based on a unified assessment of the success of dental implantation in the post-extraction zone. The aim of our study is to conduct a comprehensive comparative analysis of osteoplastic materials after preservation of the extraction wells of extracted teeth. The null hypothesis is that the ADM technique can be used in patients and the newly formed bone regenerate will be sufficient for implant placement.
CONDITIONS
Official Title
Alveolar Ridge Preservation After Tooth Extraction Using Autologous Dentin Matrix
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age from 18 to 70 years
- Indications for tooth extraction such as periapical periodontitis, root or crown fracture without possibility of rehabilitation, or chronic periodontitis
- Satisfactory oral hygiene
- Signed informed consent approved by ethics committee
You will not qualify if you...
- Under 18 years of age
- Pregnant women
- Severe comorbidity in the stage of decompensation
AI-Screening
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Trial Site Locations
Total: 1 location
1
Moscow State Univerciry of medicine and dentistry
Moscow, Russia, 123022
Actively Recruiting
Research Team
N
Nikolai Redko, PhD
CONTACT
A
Alexei Drobyshev
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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