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临床试验/CTRI/2025/03/082567
CTRI/2025/03/082567尚未招募不适用

Assessment of implant stability and bone volume around apex of implants using three different Osteotome techniques for Indirect Sinus lift procedures.

Shilpa Dandekeri1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年4月2日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Rehabilitation of patients with good function and esthetics

研究概览

简要总结

This is a randomized control trail where in  patients will be assigned to one of three groups : Fifteen patients in Summers osteotome (control group) Fifteen patients in Osseodensification  (intervention group) Fifteen patients in Summers Osteotomy with PRF group (intervention group)

For all groups, pre-operative extra-oral photograph with panoramic radiograph for initial screening will be taken. Impressions for upper and lower arches will be recorded and then face bow transfer will be accomplished. Prosthetic wax-up fabrication and pre-surgical stent will be performed for evaluation of implant placement. Moreover, for each patient, CBCT(FOV) will be performed after sinus lifting procedure (T0) and 4 months postoperatively (T1) and 4 months postoperatively (T2). Data will be acquired by standardizing CBCT(FOV) parameters (10 mA, 12 kVp, 0.4 voxel size). For analysis, Planmeca Romexis software version 4.6.2.R. will be used.

研究设计

研究类型
Interventional

入排标准

年龄范围
25.00 Year(s) 至 75.00 Year(s)(—)
性别
All

入选标准

  • 1.Patient requiring implant treatment in the maxillary arch(D3 ,D4 BONE) 2.Patient with medial and lateral sinus floor angle of more than 30 degree.
  • 3.Patients at least 25years old, providing consent for documentation and public presentation of their clinical data.
  • 4.Patients with fair Oral health Index.

排除标准

  • 1.Patients with uncontrolled diabetes, recent 2.Cardiac surgery,patients on bisphophanates 3.Patients with bleeding disorders 4.Serum glycated haemoglobin more than7.0 5.Patient with poor oral hygiene index scoresless4 6.Patients with vertigo.

结局指标

主要结局

Rehabilitation of patients with good function and esthetics

时间窗: 4years

次要结局

  • Better quality of life(20years)

研究者

发起方
Shilpa Dandekeri
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

SHILPA DANDEKERI

NITTE Deemed to be University

研究点 (1)

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