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临床试验/NCT07657364
NCT07657364招募中不适用

Prosthetic Complications in Full-arch Screw-retained Implant Restorations Using Monolithic Zirconia Versus Titanium Frameworks: A Randomized Clinical Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2026年4月12日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
12
试验地点
1

研究概览

简要总结

The goal of this clinical trial is to to compare the prosthetic complication rate and Oral Health-Related Quality of Life (OHRQoL) between screw-retained monolithic zirconia frameworks and CNC-milled titanium frameworks with zirconia superstructures in completely edentulous patients restored with full-arch implant-supported prostheses over a follow-up period of 12 months.

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

盲法说明

Single-blind (Statistician)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18 years or older.
  • Able to understand the study procedures and provide written informed consent.
  • In good general health, classified as American Society of Anesthesiologists (ASA) Physical Status Class I or II.
  • Completely edentulous in the arch to be treated (maxilla and/or mandible).
  • A candidate for a full-arch, screw-retained implant-supported prosthesis, requiring 4 to 6 implants in the treatment arch.
  • Sufficient bone volume at planned implant sites to place implants of at least 3.5mm in diameter and 8mm in length.
  • Adequate crown height space (15-22 mm) for a fixed prosthesis.
  • A zone of keratinized mucosa at the crest of the ridge measuring at least 2 mm in width.
  • Opposing arch is fixed full-arch implant-supported prosthesis.
  • Demonstrates acceptable oral hygiene and the motivation to maintain it.

排除标准

  • Medical contraindications:
  • Uncontrolled diabetes (HbA1c > 7.0%).
  • History of radiotherapy in the head and neck region.
  • History of intravenous bisphosphonate therapy.
  • Immunosuppressed or immunocompromised status.
  • Any other uncontrolled systemic disease that constitutes a contraindication for oral surgery.
  • Behavioral Factors:
  • Heavy smoking, defined as consumption of more than 10 cigarettes per day.
  • Presence of parafunctional habits (e.g., bruxism, clenching) as diagnosed by clinical examination.
  • Local Oral Factors:
  • Active, untreated periodontal disease in any remaining dentition.
  • Presence of acute oral infection or pathology at the intended surgical site.
  • Crown height space less than 15 mm or more than 22 mm.
  • Insufficient keratinized mucosa (< 2 mm width) that cannot be corrected with a simple surgical procedure prior to implant placement.
  • Pregnancy or lactation.
  • Participation in another interventional clinical trial.
  • Perceived inability to comply with the study protocol and follow-up schedule.

研究者

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

Ahmad Diab Ahmad ElSayed

PhD researcher

Cairo University

研究点 (1)

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