跳至主要内容
临床试验/jRCT1032240582
jRCT1032240582尚未招募不适用

Evaluation of the denture retention under the use of denture stability materials developed for patients with dry mouth.

not applicable0 个研究点目标入组 26 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
26
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Controlled Trial
干预模型
Crossover Assignment
主要目的
Treatment Purpose
盲法
Single Blind

入排标准

年龄范围
No limit 至 No limit(—)
性别
All

入选标准

  • Patients who visit the Oral Function Management Department at Showa University Dental Hospital
  • Patients who have had maxillary complete dentures made in our department and are undergoing regular checkups
  • Individuals who have given written informed consent to participate in this study

排除标准

  • Those with oral mucositis or other abnormal findings.
  • Persons who use drugs that affect salivary secretion on the day of measurement.
  • (tricyclic and tetracyclic antidepressants, antihypertensive drugs such as loop diuretics and calcium channel blockers, antiparkinsonian drugs such as anticholinergics and L-dopa containing preparations).
  • Persons who have experienced hypersensitivity symptoms due to the test sample.
  • Persons who have difficulty swallowing.
  • Persons who are deemed ineligible as research subjects by the investigator.

结局指标

主要结局

-

Retentive strength of duplicate denture after 30 minutes in each test sample

次要结局

  • Retentive strength of duplicate denture when test sample is not used
  • Retentive strength of duplicate denture at 0, 10, and 20 minutes for each test sample(0, 10, and 20 minutes)
  • Oral moistness
  • Results of usability questionnaire (VAS values)

研究者

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