跳至主要内容
临床试验/EUCTR2006-000789-35-CZ
EUCTR2006-000789-35-CZ进行中(未招募)1 期

Two-way Crossover Comparison of the Sensitivity and Specificity of the Modified Helicobacter Test INFAI Using New Test Meal vs. Standard 13C-Urea Breath Test in Helicobacter Pylori Positive and Negative Patients with Dyspepsia Taking Proton Pump Inhibitors

INFAI GmbH0 个研究点目标入组 115 人开始时间: 2006年8月22日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
115

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Male and female patients of at least 18 years of age
  • - All acid-related disorders requiring long-term PPI treatment including functional dyspepsia according Rome II Classification
  • - Positive or negative standard 13C-UBT at screening
  • - Diagnosis of Hp infection confirmed or excluded by combination of culture#, histology* and rapid** urease test on samples obtained bz endoscopy:
  • - True positive: culture and/or (histology and rapid urease test) are positive
  • - True negative: at least two tests are negative and culture is not positive
  • - True negative: culture not evaluable and both histologz and urease test are negative.
  • #) Culture will be based on antrum biopsies
  • *) 4 endoscopic biopsies from antrum and 1 biopsy from corpus will be sampled. Histological processing and evaluation will beperformed for at least one sample of the antrum and the corpus.
  • **) Rapid urease test will beperformed on the sampke of antrum biopsy.
  • - Written informed consent of patient
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Previous Hp eradication therapy
  • - intake of PPI, H2 receptors anatgonists, NSAIDs, antibiotics, antisecretory drugs, bismuth compounds, or sucralfate in 4 weeks prior to enrolment
  • - Manifest coagulopathy or any other disorder according to which endoscopy and/or biopsies are contraindicated.
  • - Participation in a clinical trial with another not approved drug within 30 days before entering the study and/or previous participation in this study.

研究者

发起方
INFAI GmbH

相似试验

已完成
不适用
Effct of Rehabilitation in Stroke Recoverystroke.stroke, not specified as haemorrhage or infarction
IRCT2016102430477N1Vice Chancellor of Research, Shiraz University of Medical Science20
尚未招募
不适用
The effect of prolonged dietary exposure and the association between taste receptor expression, fatty acid taste sensitivity and satiety in healthy weight participantsOverweight and obesityDiet and Nutrition - Obesity
ACTRN12612000881831Deakin University, School of Exercsie and Nutritional Sciences, Centre for Physical Activity and Nutritional Sciences35
已完成
不适用
A randomised, double-blind, crossover comparison of the efficacy and safety of study drug 017 and placebo in patients with neuropathic pain due to diabetic neuropathy (DN) or post-herpetic neuralgia (PHN)
ISRCTN33347454Purdue Pharma Canada70
进行中(未招募)
1 期
To test the hypothesis that a 4 week treatment with atomoxetine is more effective than placebo in patients with combined type Attention Deficit/Hyperactivity Disorder (ADHD), patients with only Reading Disorder, and patients with combined type ADHD and Reading Disorder.Attention-Deficit/Hyperactivity Disorder (AD/HD)MedDRA version: 23.0Level: LLTClassification code 10003735Term: Attention deficit-hyperactivity disorderSystem Organ Class: 100000004873
EUCTR2006-001866-18-Outside-EU/EEAEli Lilly and Company
已完成
不适用
Randomized crossover comparison study on the subjective evaluation (VAS) at the time of speech and the influence on the brain activity by the difference in position of the palatal bardenture user
JPRN-UMIN000030209Graduate School of Dentistry, Kanagawa Dental University25