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临床试验/NCT00388453
NCT00388453已完成不适用

ADHERE Study: Application of Dx-pH Catheter for Extra-esophageal Reflux Evaluation

Vanderbilt University Medical Center2 个研究点 分布在 1 个国家目标入组 47 人开始时间: 2006年10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
47
试验地点
2
主要终点
Decrease in pH From Baseline to <4

研究概览

简要总结

The purpose of this study is to establish the clinical application of a new device that records pH changes in the hypopharynx. The investigators also aim to compare the consistency of distal esophageal pH with hypopharyngeal pH using both the "short" and the "long" catheters in patients.

详细描述

Gastroesophageal reflux disease (GERD) has been linked to many disorders and can be diagnosed through a variety of modalities utilizing 24 hour ambulatory pH monitoring which can register the duration, pattern and symptom correlation of distal esophageal acid exposure. This can be accomplished via a catheter probe connected from outside the body and placed through a nostril, advanced past the hypopharynx and down into the distal esophagus. Or, a small pH detector temporarily implanted in the distal esophagus during endoscopy can record reflux events. However, despite available technologies, there has long been a deficiency in detecting extra-esophageal reflux in the upper esophagus/ hypopharynx. This is of interest for gastroenterologists, otolaryngologists, and pulmonologists in the evaluation of extra-esophageal reflux as a potential culprit for asthma, chronic cough, laryngitis, globus, and non-cardiac chest pain. Until now, there has not been a device sensitive enough for accurately detecting extra-esophageal reflux (EERD) and clinicians have relied upon subjective response to empiric treatment with acid reducing medications to determine whether acid reflux was at the root of the symptoms. There are currently no well designed published studies with this device to assess its role in this group of difficult to treat patients.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male and female volunteers aged 18 to 65 years old.
  • Control group: No known history of GERD or EERD or prior PPI use.
  • GERD group: Patients with known history of GERD based on prior response to either histamine inhibitors (H2 blockers) or proton pump inhibitors (PPIs) and/or endoscopic esophagitis identified at endoscopy.
  • EERD group: Patients with chronic cough, asthma and laryngeal findings felt to be GERD related.

排除标准

  • Use of H2 blockers or PPIs within one week prior to and during the study for the GERD and EERD patients. No prior PPI use is allowed for the control population.
  • Use of antacids (Rolaids, Tums, Pepto-Bismol, etc.) within one day prior to or during the study.
  • Esophageal motility abnormalities (achalasia, esophageal spasm, severe dysphagia)
  • Expected non-compliance.
  • Positive history of ongoing alcohol or tobacco use and inability to refrain from using either during study duration (24 hours).
  • Recent nasal surgery or nasal obstruction.
  • Significant medical conditions that, in the investigator's judgment, would compromise the subject's health and safety (mental disability, psychiatric impairment, inability to read or comprehend the consent form)

结局指标

主要结局

Decrease in pH From Baseline to <4

时间窗: 24 hours

The three study groups underwent dual pH measurements of the oropharyngeal as well as esophageal acid exposure employing the regular length probe for the oropharynx and the custom-designed long probe for the distal esophagus. The reason for the custom-designed esophageal measurement was to ensure that events noted in the oropharynx originated distally and were of gastric source. Measurements for the two locations were time synchronized to ensure accuracy. Calculations were based on length of time spent in upright and supine positions, and a combination of the two positions.

Decrease in pH From Baseline to <5

时间窗: 24 hours

The three study groups underwent dual pH measurements of the oropharyngeal as well as esophageal acid exposure employing the regular length probe for the oropharynx and the custom-designed long probe for the distal esophagus. The reason for the custom-designed esophageal measurement was to ensure that events noted in the oropharynx originated distally and were of gastric source. Measurements for the two locations were time synchronized to ensure accuracy. Calculations were based on length of time spent in upright and supine positions, and a combination of the two positions. Reflux event was calculated for a drop in pH from baseline to either \<4, or \<5, or \<6 and each event had to last more than 5 seconds and could not be during the meals.

Decrease in pH From Baseline to <6

时间窗: 24 hours

The three study groups underwent dual pH measurements of the oropharyngeal as well as esophageal acid exposure employing the regular length probe for the oropharynx and the custom-designed long probe for the distal esophagus. The reason for the custom-designed esophageal measurement was to ensure that events noted in the oropharynx originated distally and were of gastric source. Measurements for the two locations were time synchronized to ensure accuracy. Calculations were based on length of time spent in upright and supine positions, and a combination of the two positions. Reflux event was calculated for a drop in pH from baseline to either \<4, or \<5, or \<6 and each event had to last more than 5 seconds and could not be during the meals.

次要结局

  • Number of Reflux Events(24 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Michael Vaezi

Principal Investigatori

Vanderbilt University Medical Center

研究点 (2)

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