跳至主要内容
临床试验/NCT07319494
NCT07319494进行中(未招募)不适用

Comparison of Advanced Platelet Rich Fibrin Versus Platelet Rich Fibrin as a Gap Filling Material in Immediate Implant Placement

Beni-Suef University1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2025年6月25日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
16
试验地点
1
主要终点
Clinical evaluation

研究概览

简要总结

Study type: Clinical Trial

Goal:

The goal of this clinical trial is to learn if Advanced Platelet-Rich Fibrin (A-PRF) versus traditional Platelet-Rich Fibrin (PRF) can improve bone healing and soft tissue outcomes in patients undergoing immediate dental implant placement.

Main questions it aims to answer:

Does A-PRF provide greater buccal bone preservation compared to PRF after immediate implant placement?

Does A-PRF improve soft tissue healing and reduce postoperative complications compared to PRF?

Comparison group:

Researchers will compare A-PRF to PRF as a gap-filling material in immediate implants to see if A-PRF results in better bone and soft tissue outcomes.

Participants will:

Undergo tooth extraction followed by immediate implant placement

Receive either A-PRF or PRF as the gap-filling material in the implant site

Have CBCT scans at baseline and 6 months to measure bone thickness

Have clinical assessments of soft tissue healing and implant stability

Attend follow-up visits at 1 week, 1 month, 3 months, and 6 months post-surgery

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

入排标准

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

入选标准

  • The selected patients has a badly decayed mandibular posterior teeth which are indicated for extraction due to dental causes (periapical abscess, trauma or caries) not periodontal as diagnosed by periapical x-ray.
  • Healthy patients who are classified according to the American Society of Anesthesiologists (ASA)(2022) physical status classification as class I.
  • Patient age ≥ 20 years old.
  • Surgical site with sufficient for implant placement.
  • Sufficient interocclusal space for prosthesis.
  • Good oral hygiene.
  • Patients have thick biotype.
  • Patients have socket class I.

排除标准

  • Active periodontal diseases and periapical lesions not chronic infections.
  • Patients have parafunctional
  • History of alcohol or drug dependency, psychological factor that might affect the surgical or prosthodontic treatment.
  • Pregnant patients.
  • Patients who are not willing to complete the study.

结局指标

主要结局

Clinical evaluation

时间窗: 6 month

Implant stability will be measured by resonance frequency analysis (RFA) values expressed as implant stability quotient (ISQ) unit at 6 months post-operative

次要结局

未报告次要终点

研究者

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

Eman Magdy Ahmed

Associate Professor

Beni-Suef University

研究点 (1)

Loading locations...

相似试验