跳至主要内容
临床试验/CTRI/2025/08/093945
CTRI/2025/08/093945已完成2 期

Clinical efficacy of Albumin Prf and injectable Prf as an adjunct to scaling and root planing in the management of stage 2 periodontitis

Chennuru Sree ramya1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2025年10月1日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
34
试验地点
1
主要终点
Assessment of Clinical attachment level

研究概览

简要总结

This study is a randomized, parallel group clinical trial comparing the efficacy of AlbuminPrf and injectable Prf as an adjunct to scaling and root planing in the management of stage 2 periodontitis patients. In 2015, injectable platelet rich fibrin was developed and initially studied using a short, slow centrifugation protocol. This method allowed injectable PRF to remain in liquid form for approximately 15 to 20 minutes. The formulation was utilized in various procedures, including its combination with bone grafts to create a stable fibrin graft matrix, enhancing handling and graft stability. To address the stability limitations of platelet concentrates, a new process was introduced that involves combining the liquid portion of liquid PRF with denatured platelet poor plasma. This formulation was initially termed Albumin Concentrated albumin with the presence of a concentrate of growth factors, offering improved stability and extended clinical applicability.The process was later renamed AlbuminPRF albumin with liquid PRF.The incorporation of denatured serum albumin significantly strengthens the PRF based scaffold, resulting in an autologous, biocompatible material with improved stability and prolonged therapeutic effects.

Group 1: Albumin Prf after Scaling and root planing

Group 2: injectable Prf after Scaling and root planing

Primary and secondary outcomes will be measured at baseline and after 3 months

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
None

入排标准

年龄范围
30.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • Subjects who are apparently healthy.
  • Presence of at least 20 teeth Subjects with Stage 2 periodontitis Subjects who are willing to give informed consent.

排除标准

  • History of previous antibiotic therapy within the past 3 months Periodontal treatment in last 6 months.
  • Pregnant woman and Lactating mothers.
  • Any form of tobacco use.

结局指标

主要结局

Assessment of Clinical attachment level

时间窗: After 3months

次要结局

  • Measurement of probing depth, Plaque & gingival index(At baseline and 3 months)

研究者

发起方
Chennuru Sree ramya
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Chennuru Sree ramya

Sibar institute of dental sciences guntur

研究点 (1)

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