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临床试验/NCT02675283
NCT02675283已完成不适用

Case Finding for Coeliac Disease Using a Point of Care Test in a Pharmacy Setting: A Feasibility Study

Sheffield Teaching Hospitals NHS Foundation Trust2 个研究点 分布在 1 个国家目标入组 502 人开始时间: 2016年7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
502
试验地点
2
主要终点
The prevalence of CD in this study cohort as a result of a case finding approach using a POCT in a pharmacy setting.

研究概览

简要总结

This study aims to assess whether it is feasible to use a point of care test to increase the detection of coeliac disease in a pharmacy setting.

详细描述

Coeliac disease (CD) is an autoimmune condition characterised by mucosal damage of the small intestine by dietary gluten. CD affects 1 in 100 people. However, patients do not always have symptoms, resulting in 5 undiagnosed patients to every known case of CD. Undiagnosed CD can lead to complications such as vitamin and mineral deficiencies, osteoporosis and small bowel lymphoma, as well as impairing quality of life.

Currently, patients are diagnosed with a conventional blood test for coeliac antibodies (anti-TTG) as a first line test. Simtomax®, a new coeliac point of care test (POCT), has become available. It is a finger prick test that provides results of a coeliac antibody, deaminated gliadin peptide, within 10 minutes. Studies showed that Simtomax is as accurate as anti-TTG, with a 92.7% chance of detecting CD and 98.7% chance of ruling out CD.

This study aims to assess whether the POCT can increase the detection of adult coeliac disease when used in a pharmacy setting. A feasibility study using a case-finding approach will be conducted at 5 pharmacies in Sheffield over 20 months. It will be funded by Professor Sanders' research funds.

Customers who enter the pharmacies will be approached by the principal investigator (PI). Eligible participants (those with symptoms suggestive of or risk factors for CD) will be consented for the POCT by the PI. The POCT will be carried out at the pharmacies. Any participant with a positive test will be advised to see his GP to be referred for a gastroscopy at the Royal Hallamshire Hospital to confirm the diagnosis. Once diagnosed, the participant will follow the standard management pathway for any patients with CD.

Results of the study will be compared to the established prevalence of CD of 1%, to assess whether using POCT in a pharmacy setting can increase the detection of adult CD.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 or over, and
  • Purchasing gastrointestinal medications, including:
  • Over the counter medications (i.e. medicines purchasable without a prescription or supervision of a pharmacist)
  • Pharmacy medications (i.e. medicines purchasable from a pharmacy without a prescription but provided under the supervision of a pharmacist. These medicines are kept 'behind the counter' and are not available on the pharmacy shelves.)
  • Prescription only medications (i.e. medicines only available with a prescription that is issued by a GP or another suitably qualified healthcare professional), and/ or
  • Suffering from any of the following:
  • Persistent unexplained abdominal or gastrointestinal symptoms
  • Prolonged fatigue
  • Unexpected weight loss
  • Severe or persistent mouth ulcers
  • Unexplained iron, vitamin B12 or folate deficiency
  • Type 1 diabetes
  • Autoimmune thyroid disease
  • Irritable bowel syndrome
  • Metabolic bone disorder (reduced bone mineral density or osteomalacia)
  • Unexplained neurological symptoms (particularly peripheral neuropathy or ataxia)
  • Unexplained subfertility or recurrent miscarriage
  • Persistently raised liver enzymes
  • Dental enamel defects, and/ or 4 Have first degree relatives with coeliac disease

排除标准

  • previous diagnosis of coeliac disease, or
  • previous or current investigation for coeliac disease.
  • age under 18.

结局指标

主要结局

The prevalence of CD in this study cohort as a result of a case finding approach using a POCT in a pharmacy setting.

时间窗: Baseline - 20 months

This feasibility study will describe the prevalence of CD in this study cohort. This will be compared to the established prevalence of CD of 1% in the general population.

次要结局

  • The proportion of individuals undergoing a gastroscopy with duodenal biopsies.(Baseline - 20 months)
  • The proportion of individuals agreeing to fill in the eligibility questionnaire.(Baseline - 20 months)
  • The proportion of individuals undertaking the POCT.(Baseline - 20 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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