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临床试验/NCT05680285
NCT05680285已完成不适用

Clinical and Radiographic Evaluation of Low Level Laser Therapy in Primary Tooth Pulpotomy Treatment

Uşak University2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
90
试验地点
2
主要终点
radiographic success of treatments at the end of 12 months

研究概览

简要总结

In our study, it was aimed to compare the long-term effectiveness of diode laser and low level laser therapy and primary tooth amputation treatments using calcium hydroxide (LLLT+CH) in primary second molars with deep dentinal caries. Ninety patients ( 42 Gırl, 48 Boy) aged 6-9 years with deep dentin caries in the mandibular second molar were included in the study. The patients were randomly selected according to the treatment to be applied and divided into two groups as the diode laser group (N=45) and the LLLT+CH group (N=45). The patients were called for control appointments at the 1st, 3rd, 6th and 12th months after the treatment, and both clinical and radiographic follow-ups were performed. Chi-square and Fisher's Exact tests were used to compare categorical variables according to groups in statistical analysis, and p<0.05 was considered significant. When the study results at the end of 12 months were evaluated, the diode laser group had a clinical success rate of 95.6%, and a success rate of 93.3% radiologically; The LLLT+CH group had a success rate of 97.7% clinically and 90.9% radiologically. There was no statistically significant difference between the success rates of the groups (p>0.05). According to the clinical and radiographic results of our study, it was determined that diode laser and LLLT+CH amputations showed similar success rates in primary second molars with deep dentin caries. It has been seen that both methods can be used safely in primary tooth amputations. It is thought that clinical and histological studies and studies examining the effectiveness of dental laser applications in primary tooth amputation treatment are needed.

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
None

入排标准

年龄范围
6 Years 至 9 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Clinical Criteria
  • No systemic disease
  • Not allergic to the materials used
  • Children with scores of 1 and 2 according to the Frankel behavioral scale
  • Those who have erupted permanent first molars
  • The one in occlusion with the opposing tooth
  • Not having bad oral habits
  • No structural anomaly in the teeth
  • No spontaneous or nocturnal pain
  • No sensitivity to palpation or percussion
  • Abscess and fistula formation free
  • No pathological mobility
  • During treatment, pulp bleeding is controlled within 5 minutes.
  • With a crown that can be made of stainless steel crown (PÇK)
  • Radiographic Criteria
  • Having a deep dentin caries lesion very close to the pulp
  • No resorption in the bifurcation and periapical area
  • Periodontal space is healthy and there is no periapical region pathology
  • Absence of internal and external root resorption in roots
  • No calcified masses in the pulp
  • Teeth that did not exceed one-third of the physiological root resorption were included in the study.

排除标准

  • Children with a score of 1 and 4 on the Frankel Scale were excluded.

结局指标

主要结局

radiographic success of treatments at the end of 12 months

时间窗: 12 months

teeth without any signs of pathological internal and external root resorption, enlargement of the periodontal space, and radiolucency in the periapical and furcation region

clinical success of treatments at the end of 12 months

时间窗: 12 months

teeth without any of the signs of spontaneous pain, tenderness on palpation and percussion, pathological mobility, sinus tract or gingival abscess form, lymphodanepathy in the relevant region

次要结局

未报告次要终点

研究者

发起方
Uşak University
申办方类型
Other
责任方
Sponsor

研究点 (2)

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