Actively Recruiting
Post Extraction Changes After Alveolar Socket Preservation Using Autogenous Dentin Graft (ADG) Combined With Either Albumin Platelet-rich Fibrin (ALB-PRF) or Standard Platelet-rich Fibrin (PRF).
Led by Kafrelsheikh University · Updated on 2025-07-10
60
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study focuses on the impact of tooth loss on alveolar bone, which shrinks significantly within the first three months. To prevent this, strategies like alveolar ridge preservation are used. Autogenous dentin, taken from the patient, supports healing and bone regrowth. Platelet-rich fibrin (PRF), made from the patient's blood, enhances healing and bone density by releasing growth factors. A new technique combining L-PRF with albumin creates a stable healing membrane that provides a steady release of growth factors. Overall, these methods improve recovery after tooth extractions and prepare sites for future dental work.
CONDITIONS
Official Title
Post Extraction Changes After Alveolar Socket Preservation Using Autogenous Dentin Graft (ADG) Combined With Either Albumin Platelet-rich Fibrin (ALB-PRF) or Standard Platelet-rich Fibrin (PRF).
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Medically free patients
- Adults aged 18 to 60 years
- Non-restorable tooth needing extraction
- Tooth located in the posterior lower jaw
- No active infection related to the tooth
- Cooperative with study procedures
You will not qualify if you...
- Any systemic disease affecting therapy outcome
- Smoking, pregnancy, or lactation
- Presence of bone diseases
- Poor oral hygiene
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kaferelsheikh University
Kafr ash Shaykh, Kafrelsheikh, Egypt, 6860404
Actively Recruiting
Research Team
M
MUATH ATIF HASSAN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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