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临床试验/NCT07446790
NCT07446790招募中不适用

Scan Time and Prosthetic Complications of Intraoral Scanning Versus Intraoral Photogrammetry for Full-Arch Titanium Framework With Zirconia Overlay Implant Screw-Retained Prostheses: A Randomized Clinical Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2025年8月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
11
试验地点
1
主要终点
Scan time

研究概览

简要总结

This study aims to evaluate the effect of intra-oral scanning and intra-oral photogrammetry on scan time and prosthetic complications in patients receiving full-arch titanium framework with zirconium overlay implant screw-retained prostheses.

Participants will:

Receive a full arch implant prosthesis and scan time will be recorded. Prosthetic complications (e.g., screw loosening, framework fracture, zirconia chipping) will be recorded at 3 and 6-month follow-up period post-delivery and we will manage complications at the time of prosthetic complication occurrence.

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
Single (Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients requiring maxillary and/or mandibular full arch screw-retained implant-supported prosthesis.
  • Number of implants placed per arch ranging from 4-6 implants per arch.
  • Completely edentulous patients with sufficient inter-arch space to receive fixed prosthesis (Crown height space 9-15 mm per arch).
  • Adequate zone of keratinized mucosa (> 2mm width).
  • Both genders.
  • Acceptable oral hygiene.
  • Cooperative patients.
  • Controlled systemic diseases (Diabetes, hypertension).

排除标准

  • Completely edentulous patients with insufficient inter-arch space to receive fixed prosthesis (Crown height space lesser than 9mm per arch).
  • Completely edentulous patients with in-adequate zone of keratinized mucosa (< 2mm).
  • Un cooperative patients.
  • Poor oral hygiene.
  • Uncontrolled systemic diseases (Diabetes, hypertension).

研究组 & 干预措施

IOP will be performed using a specialized photogrammetry system. The photogrammetry data will be use

Experimental

干预措施: Intraoral photogrammetry (IOP) (Device)

IOS will be performed using commercially available IOS device. The scan data will be used to design

Active Comparator

干预措施: Intraoral scanner (IOS) (Device)

结局指标

主要结局

Scan time

时间窗: At week 1 during the clinical visit of scanning the arch and bite registration.

次要结局

  • Prosthetic complications(At 3, 6 months of delivery of final prosthesis.)

研究者

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

Nour El Hoda Mahmoud Naguib El Tarabishi

Principal Investigator

Cairo University

研究点 (1)

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