Crestal Bone Level After Allogenic Bone Ring With Simultaneous Dental Implant Placement

Cairo University (CU)

Status: Unknown

Conditions: Allogenic Bone Ring

Treatments: Procedure: allogenic bone ring; Procedure: autogenous bone ring

Study type: Interventional

Funder types: Other

Identifiers

NCT03906591

allogenic bone ring

Details and patient eligibility

About

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

Enrollment: 28 estimated patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Medically free form any systemic diseases that contraindicate the surgical procedures or affect predictable outcomes and non-smoker subjects.
2. Atrophic mandibular distal region requiring vertical augmentation.
3. Good oral hygiene and healthy keratinized mucosa.

Exclusion criteria

1. Presence of acute dentoalveolar infection or any pathologic lesions.
2. Totally edentulous patients and patients requiring massive reconstruction and augmentation procedures.
3. Patients with history of previously failed augmentation procedures, or failed implant placement at the intended augmentation region.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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28 participants in 2 patient groups

allogenic bone ring

Experimental group

Treatment:

Procedure: allogenic bone ring

autogenous bone ring

Active Comparator group

Treatment:

Procedure: autogenous bone ring