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临床试验/NCT01167543
NCT01167543已完成不适用

Relationship and Pathophysiology of Gastroesophageal Reflux and Dental/Periodontal Disease

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2005年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
79
试验地点
1

研究概览

简要总结

This study investigates the prevalence and pathophysiology of dental and periodontal involvement in pediatric patients with symptomatic or asymptomatic gastroesophageal reflux (GER) or gastroesophageal reflux disease (GERD). Primary objectives are to compare the prevalence of oral disease in children with and without a diagnosis or symptoms/signs of GERD in a cross-sectional study. Secondary objectives are to examine factors that might lead to the pathogenesis of the dental and periodontal lesions observed in this group of subjects.

The primary hypothesis is to prove that children aged 10-18 years diagnosed with or having symptoms or signs of GERD have a significantly higher amount of dental erosions in comparison to a matched control group.

Secondary hypotheses are that children aged 10 - 18 years diagnosed with or having signs of GER have higher DMFS (Decayed, Missing, Filled permanent tooth Surfaces) rates, higher SBI (Sulcus Bleeding Index) rates, worse Periodontal status, and lower saliva buffering capacity.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
9 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Ages 9.0 to 18.0 years, of either gender
  • Able to give verbal / written assent / consent themselves and/or informed consent from a parent/guardian
  • Willing to comply with all study procedures and protocols,
  • Willing to get dental photographs and impressions taken
  • Willing to sign the "Authorization for Release of Personal Health Information and Use of Personally Unidentified Study Data for Research" form

排除标准

  • Subjects suffering from systemic diseases, significant past or medical history with conditions that may affect oral health or oral flora (i.e. diabetes, HIV, heart conditions that require antibiotic prophylaxis)
  • Other conditions that may decrease the likelihood of adhering to study protocol,
  • Subjects who will leave the area and are unable to complete the study.

研究者

申办方类型
Other

研究点 (1)

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