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临床试验/NCT07418788
NCT07418788进行中(未招募)不适用

Efficacy of Polymeric Nano Calcium Fluoride Varnish, Diode Laser Individually and in Combination in the Treatment of Dentin Hypersensitivity.

Faculty of Dental Medicine for Girls1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年5月15日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
30
试验地点
1
主要终点
Pain severity

研究概览

简要总结

The aim of the study is to assess the effect of polymeric nano calcium fluoride Varnish (Oli-NANO seal), 976 nm diode laser solely and combination of both therapies in the treatment of dentin hypersensitivity

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, Outcomes Assessor)

入排标准

年龄范围
30 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Medically free
  • Non-smokers
  • Co-operative patients who will be interested in participating in the study and willing to sign the informed consent.
  • Availability of patients for 1 year

排除标准

  • Patients currently using analgesic, anti-inflammatory medications, sedatives, tranquilizers, anticonvulsants, or any other medications that could potentially alter pain perception.
  • Patients undergoing orthodontic treatment.
  • Patients using desensitizing toothpaste
  • Patients receiving dentin hypersensitivity (DH) treatment
  • Pregnant or lactating women
  • Patients have high consumption of sour and acidic food
  • Patients who had undergone professional desensitizing therapy during the previous 3 months.

研究组 & 干预措施

Group 1 (OliNano Seal)

Experimental

OliNano Seal (polymeric nano calcium fluoride containing varnish)

干预措施: Olinano seal (Other)

Group 2 (Diode laser)

Active Comparator

Diode laser

干预措施: Diode Laser (Device)

Group 3 (OliNano Seal and Diode laser)

Experimental

OliNano Seal and Diode laser

干预措施: Olinano seal and Diode Laser (Other)

结局指标

主要结局

Pain severity

时间窗: Before the treatment (Baseline), after the first session (T1), second session (T2) will be done after a week from the first session, after 3 months (T3), 6 months (T6), 9 months (T9) and 12 months (T12)

The pain will be assessed using the (VAS) scale. The VAS is a scale that allows the patient to self-assess the pain felt by means of a line in which the patient marks the pain level "no pain" to the "maximum pain". 0: low pain, 1 - 3: moderate pain: 4 - 6, intense pain: 7 - 9, extremely intense pain: 10

次要结局

未报告次要终点

研究者

发起方
Faculty of Dental Medicine for Girls
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Bassant Bahaa El Din Ibrahim

Assistant Lecturer of Restorative Dentistry

Misr International University

研究点 (1)

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