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临床试验/CTRI/2024/08/072547
CTRI/2024/08/072547尚未招募2/3 期

Clinico- Radiological Evaluation of Dentinal Graft against Platelet Rich Fibrin in Extraction Sockets with Immediate Implant Placement- A Randomized Control Trial.

Datta Meghe Institute of Higher Education and Research1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年8月27日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
The success of the implant will be determined by the crestal bone changes and stability after 6 months following the use of DENTINAL GRAFT and PRFM

研究概览

简要总结

Dental implant therapy has advanced significantly, providing consistent outcomes for patients. While reduced residual ridge height is common with delayed loading implants, various procedures prevent post-extraction alveolar ridge resorption. These include socket grafting materials, for bone regeneration, and instantaneous implant placement. Flapless surgery preserves bone vascularization, reducing the need for multiple surgeries and enhancing. Atraumatic extraction minimizes tissue stress, protecting remaining bone. Peri-implant voids often occur due to the horizontal gap distance between the implant and alveolar socket This study aims to evaluate the efficacy of Dentinal graft (DG) against Platelet rich fibrin matrix (PRFM) in immediate  implant procedures utilizing a two-stage protocol. This will be a prospective randomized controlled trial will be conducted, wherein patients fulfilling the inclusion criteria will be equally divided into two groups. Group A will comprise of patients in which DENTINAL graft will be placed before implant placed in freshly prepared socket after extraction‘, whereas in Group B patients will receive PRFM. After extraction socket Functional Outcomes will be measured using parameters like Clinical and Radiographic measurement The success of the implant will be determined by the crestal bone changes and stability after 6 months following the use of PRFM and DENTINAL GRAFT.

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 Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • 1.All patient undergoing mandibular posterior teeth extraction with immediate implant placement.
  • 2.All patients with radiographic and clinical evidence suggestive of intact alveolar osseous architecture 3.Presence of at least 2 mm of bone beyond the root apex (Above canal).
  • 4.Patients with type I extraction sites (four-wall socket) as per Salama and Salama (1993) classification.

排除标准

  • 1 All patients with underlying systemic health conditions that may impede the osseous healing cascade, such as diabetes, osteoporosis, hematologic disorders, and titanium allergies.
  • 2.All patients with D-4 bone quality.

结局指标

主要结局

The success of the implant will be determined by the crestal bone changes and stability after 6 months following the use of DENTINAL GRAFT and PRFM

时间窗: Assessment will be done at 3rd and 6th month

次要结局

未报告次要终点

研究者

发起方
Datta Meghe Institute of Higher Education and Research
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Krishna Pampatwar

Datta Meghe Institute of Higher Education & Research

研究点 (1)

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