NCT03906591
Unknown
Not Applicable
Evaluation Of Crestal Bone Level After Alveolar Bone Augmentation of Atrophied Posterior Mandibular Region Using Allogenic Bone Rings Vs. Autogenous Bone Rings With Simultaneous Dental Implant Placement (A Randomized Controlled Clinical Trial)
ConditionsAllogenic Bone Ring
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Allogenic Bone Ring
- Sponsor
- Cairo University
- Enrollment
- 28
- Primary Endpoint
- change in crestal bone height
- Last Updated
- 7 years ago
Overview
Brief Summary
This trial is aiming to answer a question whether in Patients with severely atrophied, distal mandibular regions, the use of allogenic bone rings with simultaneous dental implants, compared to autogenous bone rings, give successful clinical and radiographic outcomes without donor site morbidity
Investigators
Alaa El-Deen Ragab Mahmoud
principal investigator
Cairo University
Eligibility Criteria
Inclusion Criteria
- •Medically free form any systemic diseases that contraindicate the surgical procedures or affect predictable outcomes and non-smoker subjects.
- •Atrophic mandibular distal region requiring vertical augmentation.
- •Good oral hygiene and healthy keratinized mucosa.
Exclusion Criteria
- •Presence of acute dentoalveolar infection or any pathologic lesions.
- •Totally edentulous patients and patients requiring massive reconstruction and augmentation procedures.
- •Patients with history of previously failed augmentation procedures, or failed implant placement at the intended augmentation region.
Outcomes
Primary Outcomes
change in crestal bone height
Time Frame: at 6 months
cone beam computed tomography will be used to measure bone height in millimeters
Secondary Outcomes
- implant loss(after 1 week, 6 months and after 9 months)
- graft failure(after 1 week, 6 months and after 9 months)
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