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临床试验/NCT07212985
NCT07212985已完成不适用

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

Al-Azhar University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年1月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
Change in horizontal alveolar ridge width

研究概览

简要总结

. 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

详细描述

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

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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

排除标准

  • •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

研究组 & 干预措施

ABG + Xenograft + Collagen Membrane

Experimental

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).

干预措施: Autogenous Bone Block + Xenograft + Collagen Membrane (Procedure)

ABG + EthOss (Synthetic Graft)

Experimental

Patients receive autogenous bone block graft (from chin) combined with EthOss, a biphasic synthetic graft material (35% calcium sulfate, 65% β-tricalcium phosphate).

干预措施: Autogenous Bone Block + Xenograft + Collagen Membrane (Procedure)

结局指标

主要结局

Change in horizontal alveolar ridge width

时间窗: Baseline, 1 week, and 6 months post-surgery

次要结局

  • Postoperative complications(Up to 6 months post-surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nora Abdelgawad Mohamed

Associate Professor of Oral Medicine, Periodontology and Diagnosis, Faculty of Dental Medicine for girls, Al -Azhar University, Cairo, Egypt

Al-Azhar University

研究点 (1)

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