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临床试验/NCT07596667
NCT07596667尚未招募不适用

Profiling Gingival Crevicular Fluid β-Catenin Level With 8-OHdG and Total Antioxidants Capacity During Healing of Periodontal Pockets: A 3-month Clinical Trial

Zeyad Nazar0 个研究点目标入组 21 人开始时间: 2026年7月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
21
主要终点
periodontal pocket depth

研究概览

简要总结

Background: To profile gingival crevicular fluid (GCF) β-Catenin, 8-OHdG, and total antioxidants capacity (TAC) in periodontitis patients during healing of periodontal pockets following non-surgical periodontal therapy (NSPT).Methods: Periodontitis patients (n = 21) will included in this clinical trial. Clinical periodontal parameters will recorded and GCF samples will collected from randomly selected 4-6 mm periodontal pockets at baseline (T0) as well as 4 weeks (T1) and 12 weeks (T2) after NSPT. GCF levels of β-catenin, 8-OHdG, and TAC will be assayed by enzyme linked immunosorbent assay (ELISA).

详细描述

Background: To profile gingival crevicular fluid (GCF) β-Catenin, 8-OHdG, and total antioxidants capacity (TAC) in periodontitis patients during healing of periodontal pockets following non-surgical periodontal therapy (NSPT).Methods: Periodontitis patients (n = 21) will included in this clinical trial. Clinical periodontal parameters will recorded and GCF samples will collected from randomly selected 4-6 mm periodontal pockets at baseline (T0) as well as 4 weeks (T1) and 12 weeks (T2) after NSPT. GCF levels of β-catenin, 8-OHdG, and TAC will be assayed by enzyme linked immunosorbent assay (ELISA).

Keywords: periodontal diseases; periodontal debridement; dental polishing; periodontal pocket

Why is this important?

This research explained the effects of non surgical periodontal treatment for patients with periodontal disease on the epithelial tissue regeneration during the healing process.

Introduction Periodontitis is a destructive disease of tooth-supporting tissues which initiated in response to frank dysbiosis of dental biofilm complemented by aggravated immune response. The hallmark of periodontitis is pathologic deepening of gingival sulci which are transformed into periodontal pockets when the front of dental biofilm advances apically. In such situation, immune responses are initiated within gingival tissue in order to counterattack the pathobionts and its virulent products . Polymorph nuclear cells, mainly neutrophils, are among the principle immune system components responsible for this task via series of biological activities such as phagocytosis and netosis. Prolonged inflammation of periodontal lesions and continuous heavy recruitment of these inflammatory cells leads to the release of oxygen free radicals (ROS) in an escalating pace which overwhelm antioxidant capacity of the host . Overproduction of ROS trigger series of destructive events characterized by increased metabolites of lipid peroxidation, DNA damage and protein damage that led to tissues damage . This shift of oxidative-antioxidant balance towards oxidative stress leads to dramatic changes in the levels of oxidative stress-related molecules such as total antioxidant capacity (TAC) and 8-hydroxy-2'-deoxyguanosine (8-OHdG) . These biomarkers can be clinically detected in oral biofluids such as saliva and GCF with a potential to discriminate between periodontal health and disease .

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • patients over 18 years old
  • patients with periodontal pockets depth more than 4 mm

排除标准

  • Pregnant women
  • patients taking antibiotic within the last three months
  • Patients with systemic disease ( Diabetes mellitus)

研究组 & 干预措施

periodontitis patients with pocket depth

Experimental

干预措施: scaling and root planing (Procedure)

结局指标

主要结局

periodontal pocket depth

时间窗: 3 months

periodontal pocket depth reduction

measurement of probing pocket depth (PPD)

时间窗: 3 months

measuring probing pocket depth (PPD)

measurement of clinical attachment loss (CAL)

时间窗: 3 months

clinical attachment loss (CAL)

次要结局

  • GCF levels of β-catenin, 8-OHdG, and TAC will be assayed by enzyme linked immunosorbent assay (ELISA) in which all have the same measuring units(3 months)

研究者

发起方
Zeyad Nazar
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Zeyad Nazar

Assistant Professor

Babylon University

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