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
- Conditions
- Implant Dentistry
- Registration Number
- NCT07212985
- Lead Sponsor
- Al-Azhar University
- Brief Summary
. 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
- Detailed 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
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- 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
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Change in horizontal alveolar ridge width Baseline, 1 week, and 6 months post-surgery
- Secondary Outcome Measures
Name Time Method Postoperative complications Up to 6 months post-surgery
Trial Locations
- Locations (1)
Faculty of Oral and Dental Medicine, Nahda University,Taibah University
🇪🇬Cairo, Egypt
Faculty of Oral and Dental Medicine, Nahda University,Taibah University🇪🇬Cairo, Egypt