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临床试验/ISRCTN76017289
ISRCTN76017289进行中(未招募)未知

Assessing the patient impact and burden of current care pathways in Barrett’s Oesophagus

Wrightington, Wigan And Leigh NHS Foundation Trust0 个研究点目标入组 750 人开始时间: 2017年11月1日最近更新:

试验速览

阶段
未知
状态
进行中(未招募)
入组人数
750

研究概览

简要总结

2017 Results article in https://pubmed.ncbi.nlm.nih.gov/28867477/ results (added 09/11/2020) 2019 Results article in https://pubmed.ncbi.nlm.nih.gov/30430714/ results (added 09/11/2020) 2019 Results article in https://pubmed.ncbi.nlm.nih.gov/31205652/ results (added 09/11/2020) 2020 Results article in https://pubmed.ncbi.nlm.nih.gov/32337055/ results (added 09/11/2020)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Must have capacity to give informed consent
  • 2. >18 years old. No upper age limit.
  • 3. Male or Female
  • 4. Meet the diagnostic criteria for each group
  • 4.1. Non-Dysplastic Barrett’s Oesophagus. All patients enrolled in surveillance who have been given a diagnosis of BO irrespective of current histology (lack of intestinal metaplasia on latest biopsies is not a criterion for exclusion providing future surveillance is indicated/recommended)
  • 4.2. Barrett’s oesophagus with dysplasia or early oesophageal adenocarcinoma. Any patient with BO diagnosed with low grade dysplasia, high grade dysplasia or early OAC eligible for ET.
  • 4.3. Colonic Polyps. Participants currently undergoing endoscopic surveillance for colonic polyps
  • 4.4. Gastro-oesophageal reflux disease. Participants without BO who have been diagnosed with any of the following; gastroesophageal reflux + oesophagitis”, gastroesophageal reflux – oesophagitis”, gastroesophageal reflux disease”, GORD”, acid reflux” or heartburn”, dyspepsia”.
  • 4.5. Normal Healthy Individuals. Population control participants who do not exhibit significant co-morbidities

排除标准

  • 1. Lack capacity to consent
  • 2. <18 years old

研究者

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