跳至主要内容
临床试验/CTRI/2025/07/092076
CTRI/2025/07/092076尚未招募不适用

Comparative evaluation of Propolis containing dentifrice and standard dentifrice as an adjunct to oral prophylaxis in plaque induced gingivitis patients A Randomized controlled trial

Dr Shruti Anna Karande1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年8月18日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
To compare and evaluate the clinical and microbiological analysis of Probing depth, bleeding on probing and plaque index

研究概览

简要总结

This is a randomized controlled trial for assessing and comparing the two different dentifrices one is Propolis containing and other is commonly used among patients. And do the clinical and microbiological analysis. This study is done for thesis of postgraduation. The aim of the study is to compare propolis containing toothpaste with common toothpaste. This will be done in patient with plaque induced gingivitis. It will be done after scaling and root planing

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • Patients above the age of 18 years of either sex.
  • 2.Patients with at least 20 teeth present.
  • 3.Patients who are systemically healthy.
  • 5.Patients characterized by a gingival index score of at least 1.

排除标准

  • Patients with any systemic diseases, which may affect the gingival status.
  • Patients who had used antibiotics, anti-inflammatory agents in the past 3 months.
  • Patients with any form periodontitis (clinical attachment loss).
  • Pregnant or lactating women.
  • Tobacco users in any form.
  • Patients with known allergy to honey and honey products.
  • Patients with any orthodontic appliances or prosthesis that would interfere with the evaluation.
  • Subjects using mouthwash or any other chemical anti-plaque agent as adjunctive oral hygiene methods.

结局指标

主要结局

To compare and evaluate the clinical and microbiological analysis of Probing depth, bleeding on probing and plaque index

时间窗: From Baseline to 1 month and then 3 month follow up

次要结局

未报告次要终点

研究者

发起方
Dr Shruti Anna Karande
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Shruti Anna Karande

Bharati Vidyapeeth Dental College and Hospital, Navi Mumbai

研究点 (1)

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