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Horizontal Anterior Maxillary Ridge Augmentation Using Autogenous Ring Block Grafts Combined With Particulate Xenogeneic Bone Versus Biphasic Beta-tri-calcium Phosphate Sulphate EthOss Graft: A Clinical Study

A

Al-Azhar University

Status

Completed

Conditions

Implant Dentistry

Treatments

Procedure: Autogenous Bone Block + Xenograft + Collagen Membrane

Study type

Interventional

Funder types

Other

Identifiers

NCT07212985
REC-PD-24-22

Details and patient eligibility

About

. Group A, received ABG cylinders obtained from the chin and organic bovine bone mineral particles (Bio-Oss xenograft) along with an absorbable collagen membrane. ABG cylinders from the chin and biphasic alloplastic (EthOss) grafting material made of CS (35%) and TCP (65%) were given to Group B. CBCT scans were conducted before bone augmentation surgery, one week and 6 months postoperatively

Full description

Two groups of forty patients participated in this prospective, controlled, randomized clinical investigation. Group A, received ABG cylinders obtained from the chin and organic bovine bone mineral particles (Bio-Oss xenograft) along with an absorbable collagen membrane. ABG cylinders from the chin and biphasic alloplastic (EthOss) grafting material made of CS (35%) and TCP (65%) were given to Group B. CBCT scans were conducted before bone augmentation surgery, one week and 6 months postoperatively

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults ≥18 years requiring implant-supported restoration in the anterior maxilla

Horizontal alveolar bone deficiency <4 mm (Cawood & Howell Class III-IV)

Satisfactory oral hygiene

No previous bone augmentation at study site

Exclusion criteria

  • Uncontrolled systemic diseases

History of head/neck irradiation or immunosuppression

Oral lesions (e.g., lichen planus)

Ongoing or recent IV bisphosphonate therapy

Untreated periodontitis or poor oral hygiene

Parafunctional habits, pregnancy, psychiatric disorders

Recent tobacco use

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

ABG + Xenograft + Collagen Membrane
Experimental group
Description:
Patients receive autogenous bone block graft (from chin) combined with particulate bovine xenograft (Bio-Oss, Geistlich Pharma AG) and covered with absorbable collagen membrane (Bio-Gide).
Treatment:
Procedure: Autogenous Bone Block + Xenograft + Collagen Membrane
ABG + EthOss (Synthetic Graft)
Experimental group
Description:
Patients receive autogenous bone block graft (from chin) combined with EthOss, a biphasic synthetic graft material (35% calcium sulfate, 65% β-tricalcium phosphate).
Treatment:
Procedure: Autogenous Bone Block + Xenograft + Collagen Membrane

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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