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. 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
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Inclusion criteria
Horizontal alveolar bone deficiency <4 mm (Cawood & Howell Class III-IV)
Satisfactory oral hygiene
No previous bone augmentation at study site
Exclusion criteria
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
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Interventional model
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40 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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