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Clinical Trials in Egypt / NCT06457373
Recruiting Not applicable

Demineralized Dentin Allograft Versus Demineralized Dentin Autograft for Socket Preservation

NCT06457373 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-08-13
Last updated
2026-08-18

Condition(s) studied

Alveolar Bone Loss

Investigational drug(s) / intervention(s)

Demineralized Dentin AllograftDemineralized Dentin Autograft

Demineralized Dentin Allograft: 20 sockets are randomly allocated to receive the Demineralized Dentin Allograft (split-mouth study)

Demineralized Dentin Autograft: 20 sockets are randomly allocated to receive the Demineralized Dentin Autograft (split-mouth study)

Study summary

This study is designed to evaluate and compare clinically and radiographically the effectiveness of Demineralized Dentin Allograft (DDA) versus Demineralized Dentin Autograft (Auto-DD) for preservation of alveolar ridge dimensions after surgical extraction of the impacted mandibular third molar.

Eligibility

Sex
ALL
Min age
25 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Patients aged between 25 to 35 years old. 2. Patients scored as (ASA I). 3. No adverse habits such as smoking, tobacco chewing, alcohol. 4. Patients having bilaterally impacted mandibular third molar with similar degree of difficulty according to (Kim JY, et al). 5. The recipient alveolar sockets are free of any pre-existing periapical pathology, based on x-ray. 6. Alveolar sockets with a depth of 5 mm or more, using periodontal probe for assessment. 7. Patients sign a consent for all procedures. Exclusion Criteria: * 1\) Pregnant or lactating patients. 2) Relevant systemic diseases. 3) Patients with history of chemotherapy or radiotherapy.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry- Horus University in Egypt Damietta New-Damietta Recruiting

More Horus University trials in Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06457373 on ClinicalTrials.gov ↗ ← All trials in Egypt