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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04393714
Other study ID # ARP2020
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 1, 2020
Est. completion date October 31, 2021

Study information

Verified date July 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The reduction in alveolar bone dimensions is an inevitable outcome after tooth extraction due to the healing events that results in bone modeling/remodeling. Alveolar ridge preservation is a successful approach that aids in reducing these changes greatly. Various techniques have been employed to achieve that outcome utilizing bone grafts and/or membrane. Dentin graft is a promising type that can overcome many of the limitations facing mainstream grafts. Autogenous source serve the advantage of providing graft with no cross-infection risk or immunogenicity. Moreover, the unique structure of dentin makes it suitable for osteoinduction and osteoconduction that yields favorite bone regeneration outcomes. Demineralization of dentin is essential to release trapped growth factors, expose collagen fibrils and enhance the grafts degradability and replacement by native tissues. Many acids have been investigated for the use in chairside preparation of the dentin graft and hence, clinicians are faced with different choices but little evidence regarding the acid which yield s better outcomes.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 8
Est. completion date October 31, 2021
Est. primary completion date August 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Non-restorable teeth

- medically healthy

- able to provide informed consent and attend follow-up period

Exclusion Criteria:

- pregnant

- smokers or alcoholic

- severe bone loss

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Alveolar ridge preservation after extraction
atraumatic extraction followed by graft material insertion

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary Radiographic bone changes width and height losses (quantitative in mm) 6 months
Secondary histological analysis Histologic observations (qualitative) and histomorphometric measurements (quantitative in %) 6 months
Secondary soft tissue healing rate of wound epitheliallization Biweekly for 6 weeks
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