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临床试验/NCT04382261
NCT04382261已完成不适用

Impact of Periodontal Bacteria at Baseline on the Effectiveness of Periodontal Therapy Outcomes in Patients With Periodontitis: A Prospective Clinical and Microbial Study

University of Messina2 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2018年6月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
102
试验地点
2
主要终点
Clinical Attachment level

研究概览

简要总结

In light of the controversy that are already approved but that however still exists regarding the efficacy and influence of the protocols for the management of Periodontitis, the aim of this study was to evaluate, at 6 months follow-up, the post-treatment clinical parameters and immunological and gingival microbial profiles in patients with periodontitis, treated by either SRP in addition to full mouth scaling or quadrant scaling

详细描述

This trial was conducted in accordance with the World Medical Association's Declaration of Helsinki of 1975, and reviewed in 2008. The local ethical committee of the University of Messina approved the study protocol and each patient was carefully informed about the possible inherent risks of the study and provided their informed written consent 102 patients, , aged 27 to 65 (mean age 44.2) were assessed for eligibility. In all subjects, subgingival plaque was acquired from 4 separate proximal sites at 180 days after therapy.

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
Double (Participant, Investigator)

入排标准

年龄范围
30 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • good condition of general health,
  • a minimum of 2 teeth for each quadrant with a Pocket Depth (PD) ranging from 4-6 mm,
  • no involvement of the furcation,
  • a minimum of a six teeth per quadrant, respectively.

排除标准

  • periodontal therapy during the last 12 months,
  • assumption of antibiotics during the last 6 months,
  • any systemic condition which might affect the effects of the study treatment,
  • previous or current radiation or immunosuppressive therapies,
  • use of mouthwash containing antimicrobials during the previous 3 months,
  • no use of hormonal contraceptives,
  • medication by anti-inflammatory and immunosuppressive drugs,
  • previous history of hard-drinking,
  • class II and III tooth mobility.

结局指标

主要结局

Clinical Attachment level

时间窗: 180 days

Analysis of reduction of clinical attachment level

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

Gaetano Isola, DDS, PhD

Researcher

University of Messina

研究点 (2)

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