跳至主要内容
临床试验/NCT03518905
NCT03518905Unknown不适用

Radiofrequency Ablation for the Treatment of Large Symptomatic Heterotopic Gastric Mucosa - a Prospective Randomized Sham-controlled Trial - the RAGE Study

Medical University of Vienna2 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2018年4月16日最近更新:
适应症

试验速览

阶段
不适用
入组人数
44
试验地点
2
主要终点
Normalization of the Reflux Symptom Index

研究概览

简要总结

The heterotopic gastric mucosa found in the cervical esophagus was first described in 1805 and affects 10-15% of individuals undergoing esophagogastroduodenoscopy. It leads to laryngopharyngeal reflux (LPR), which causes symptoms like globus sensation, hoarseness and chronic cough. The Reflux Symptom Index (RSI) that ranges from 0-45 measures LPR. Scores greater than 13 are considered to be pathologic. Currently, patients that suffer from symptoms of LPR and present with a heterotopic gastric mucosa are routinely offered radiofrequency ablation (RFA) as curative treatment. Up to now, around 40 patients were already treated at the department of Surgery with 90% histologic eradication rates after 2 treatment sessions and no reported serious adverse event. Nevertheless, the placebo effect could also be responsible for perception of improving symptoms. Therefore, this prospective sham-controlled trial was designed to exclude the placebo effect. As the device is already approved and routinely used for focal ablation safety data are already available. Up to now, there were no major adverse events, whereas only 10% of patients describe a sensation of irritated throat that dissolves within the first three days after treatment.

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
Single (Participant)

盲法说明

Patients are blinded either to sham or treatment and unblinded after 24 weeks after final examination

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histological proven presence of heterotopic gastric mucosa,
  • pathologic Reflux Symptom Index (>25)
  • age: 18-70
  • presence of symptoms > 6 months,
  • no effect on the Reflux Symptom Index to 12 weeks of standard dose proton pump inhibitor treatment
  • negative symptom correlation for symptoms with reflux events in ambulatory pH monitoring

排除标准

  • Not willing to participate in this study
  • pregnancy
  • lactation period

结局指标

主要结局

Normalization of the Reflux Symptom Index

时间窗: 6 months after first RFA treatment/or sham procedure

Normalization of the Reflux Symptom Index (RSI \<14) after two treatment/sham sessions evaluated 3 months after the second (sham-) treatment (therefore 6 months after the first endoscopy with/without RFA). Proton-pump inhibitors are paused 8 weeks before assessment

次要结局

  • Reflux Finding Score(Evaluated at the first intervention at study completion after 6 months)
  • Histological eradication rate after radiofrequency ablation or sham treatment(6 months after first RFA treatment/or sham procedure)
  • SF-12 quality of life(At enrollment (therefore before ablations or sham treatment) and 6 months after first radiofrequency ablation/sham treatment)

研究者

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

Dr. Ivan Kristo

MD, Attending surgeon, Vize-Chair of the esophageal functional testing laboratory

Medical University of Vienna

研究点 (2)

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