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临床试验/CTRI/2026/01/101271
CTRI/2026/01/101271
尚未招募
不适用

Clinical Evaluation of Conventional versus Osseodensification Drilling in Implant Placement

Individual Ayush Chettri1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2026年2月14日最近更新:

概览

阶段
不适用
状态
尚未招募
发起方
Individual Ayush Chettri
入组人数
20
试验地点
1
主要终点
assess primary stability and potentially increase bone density around the implant site prepared using osseodensification drills

概览

简要总结

Clinical Evaluation of Conventional vs. Osseodensification Drilling in Implant Placement’ aims to compare the clinical outcomes of two implant drilling techniques—conventional drilling and osseodensification. The study focuses on assessing which method provides better implant stability and bone preservation during dental implant placement. Conventional drilling removes bone to create the implant site, which can reduce bone density and compromise implant stability, particularly in areas with low bone quality. In contrast, osseodensification is a newer technique that uses specially designed burs to preserve and compact the bone during osteotomy, potentially improving both primary stability and long-term outcomes. The objectives of the study are to compare soft tissue parameters such as implant probing depth, healing index, plaque index, and bleeding index, as well as hard tissue parameters like marginal bone levels, both clinically and radiographically. The study will include adult patients who require dental implants and meet the inclusion criteria of good general and oral health. Patients with conditions affecting bone metabolism, smokers, pregnant women, and those with poor oral hygiene or a history of radiation therapy will be excluded from the study. A randomized clinical trial design will be used, with participants divided into two groups—one receiving implants via conventional drilling and the other via osseodensification. Clinical and radiographic evaluations will be post-operatively using tools such as CBCT and RVG.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Investigator Blinded

入排标准

年龄范围
20.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients who are willing to comply with all the study related procedures after signing an informed consent form.
  • Both males and females patients will be taken.
  • Non-contributing medical history.
  • Good oral hygiene.
  • Edentulous area requiring implant placement.

排除标准

  • Systemic diseases Taking medication that effect bone formation.
  • Oral mucosal lesions.
  • History of radiation therapy.
  • Alcoholics, smokers.
  • Severe bruxism Poor oral hygiene Pregnancy.

结局指标

主要结局

assess primary stability and potentially increase bone density around the implant site prepared using osseodensification drills

时间窗: 1 year

次要结局

  • enhanced secondary stability and improved bone to implant contact(1 year)

研究者

发起方
Individual Ayush Chettri
申办方类型
Other [self sponsored]
责任方
Principal Investigator
主要研究者

Ayush Chettri

Himachal Institute of Dental Sciences, Poanta Sahib,Himachal Pradesh.

研究点 (1)

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