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临床试验/CTRI/2024/05/068158
CTRI/2024/05/068158尚未招募4 期

Efficacy Comparison of the Diode Laser and Iontophoresis with 2% NaF in the management of Dentinal hypersensitivity: An in- vivo study

Dr Disha Hirani1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年6月15日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
80
试验地点
1
主要终点
The primary outcome of this study is to evaluate reduction in VAS score

研究概览

简要总结

The perplexing problem of dentin hypersensitivity (DH) has long bemused the dental profession. It is one domain where the elusive “gold standards” for its management has not yet been achieved.

Difficulties in the treatment of the DH gave rise to many protocols and therapeutic procedures which are currently being used for the improvement of DH treatment.

NaF (Sodium Flouride) Iontophoresis a method where fluoride is transferred deep into the dentinal tubules under electrical pressure. This causes calcium fluoride precipitation, which decreases fluid movement induced by stimuli, reducing dentin hypersensitivity.

Use of Laser provides an innovative and quicker treatment which results in minimal side effects and safe for the patients. Laser stimulates the odontoblasts, produces reparatory irregular dentin and obliterates the dentinal tubules which reduces the dentinal hypersensitivity. Diode Laser has specific wavelengths (655 nm to 980 nm) resulting safe for the patient and causing minimum side effects or damage to the pulp, compared to powerful systems such as Er, Cr:YSGG or Er: YAG lasers.

 Thus, the aim this study is to evaluate and compare the efficacy of diode laser and Iontophoresis with 2% NaF gel in the treatment of dentinal hypersensitivity.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

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

入选标准

  • An age limit between 20 and 50 years, irrespective of the gender.
  • Patients having sensitive permanent teeth surfaces [buccal/facial aspects of incisors, canines, or premolars] with wasting diseases and/or gingival recession having sensitivity to air blast/ visual analog scale score (VAS) ≥ 3 and ≤
  • No history of periodontal therapy in the previous 3 months.
  • Good systemic health of the selected patients with clinically elicitable DH.

排除标准

  • .Currently undergoing desensitizing treatment.
  • Caries, Pulp pathologies, defective restorations,fracture 3).
  • Chronic severe periodontal disease.
  • Uncontrolled systemic diseases.
  • .patients having pacemakers.
  • .Pregnant and/or lactating women.
  • Usage of analgesic, anticonvulsants, sedatives, tranquilizers, and anti inflammatory drugs within 72 h.

结局指标

主要结局

The primary outcome of this study is to evaluate reduction in VAS score

时间窗: baseline, immediately after the treatment, 1 week, 1 and 3 months of the recall period.

次要结局

  • reduction in tactile sensitivity(baseline, immediately after the treatment, 1 week, 1 and 3 months of the recall period.)

研究者

发起方
Dr Disha Hirani
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Disha Hirani

Hitkarini Dental College & Hospital, Jabalpur, Madhya Pradesh

研究点 (1)

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