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NCT Number: NCT02112214

Helicobacter Pylori Eradication for Gastric Cancer Prevention in the General Population

The aim of this study is to define the role of H. pylori eradication in the prevention of gastric cancer and its precursors in the context of a population-based endoscopic screening program.

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This study is active but is not currently recruiting participants.

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Key information

Age range

40 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Kosin University Gospel Hospital, Busan, South Korea

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About this study

Despite the decreasing incidence observed in the US and West European countries, gastric cancer is still an important global public health problem, especially in East Asian countries, where the burden of the disease is substantial. In the Republic of Korea, gastric cancer remains the leading cause of cancer in men and the fourth most common cancer in women. There is sufficient epidemiological and experimental evidence supporting a causal link between bacterial infection with H. pylori and gastric cancer development. However, evidence from clinical trials on the efficacy of H. pylori eradication with antimicrobial therapy to reduce the risk of gastric cancer is still limited. In addition, the beneficial or deleterious health impact of mass eradication at the population level has not been defined. In Korea, the prevalence of H. pylori infection in adults is still relatively high (~60%, >16 years old), and despite important reductions in mortality attributed to the screening program, incidence of gastric cancer remains elevated.

The investigators propose to conduct a randomized controlled clinical trial in Korea to evaluate the efficacy of H. pylori eradication to prevent gastric cancer incidence in different population subgroups including age and baseline gastric pathology. This study will be conducted in the context of the National Cancer Screening Program and the Korean Central Cancer Registry.

The proposed study will be a collaborative investigation between the National Cancer Center, Korea and the International Agency for Research on Cancer of the World Health Organization.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women aged 40-65 who are invited to participate in the National Cancer Screening Program and receive upper endoscopy
  • Willingness to sign an informed consent form
  • Good health, as determined by medical history and physical examination at enrollment

Exclusion criteria

  • Personal history of gastric cancer
  • Family history of gastric cancer in a first degree relative
  • Diagnosis and active treatment for other organ cancer except carcinoma in situ within 5 years
  • Current treatment for serious medical condition which could hinder participation (such as liver cirrhosis, renal failure, pulmonary dysfunction including COPD or asthma, or uncontrolled infection)
  • Inadequate cardiovascular function including (a) New York Heart Association class III or IV heart disease, (b) unstable angina or myocardial infarction history, (c) history of significant ventricular arrhythmia requiring medication with antiarrhythmics, and (d) history of cerebrovascular accident
  • Requirement for therapeutic anticoagulant therapy, aspirin
  • Gastric resections due to benign disease
  • H. pylori eradication therapy history
  • Mental incompetence to understand and sign informed consent
  • Alcoholism, drug abuse
  • Serious chronic diseases according to the evaluation of the study physician
  • Presence of a contraindication to the use of eradication treatment regimens
  • Inability to provide an informed consent
  • Pregnant or lactating women
  • Treatment required due to peptic ulcer, gastric cancer or esophageal cancer identified during the endoscopic examination

Treatment and study plan

10-day bismuth-based quadruple therapy

Drug

Bismuth 300 mg (4 times a day), lansoprazole 30 mg (twice a day), metronidazole 500 mg (3 times a day), and tetracycline 500 mg (4 times a day) for 10 days

Other names: Bismuth-based quadruple therapy

Placebo

Other

Placebo for bismuth-based quadruple therapy

Primary outcomes

  1. The incidence of gastric cancer between the intervention and placebo groups

    Time frame: Up to 10 years After H. pylori eradication

    Histologically confirmed gastric adenocarcinoma stage 1A or more advanced defined at endoscopy or through cancer registry

Secondary outcomes

  1. Incidence of gastric dysplasia

    Time frame: Up to 10 years After H. pylori eradication

    Diagnosis of histologically confirmed gastric dysplasia

  2. Occurrence of adverse events caused by antibiotic treatment

    Time frame: During 10 days of H. pylori eradication, and Up To 1 month after the treatment completion

    Solicited/unsolicited adverse events

  3. Incidence and mortality from other medical conditions such as obesity, diabetes, circulatory diseases, oesophageal diseases as well as other cancers and cognitive impairment

    Time frame: Up to 10 years After H. pylori eradication

    Assessed through record linkage or direct assessment during screening visits

  4. Mortality from gastric cancer

    Time frame: Up to 10 years after eradication

    Cancer registry or other reports

  5. All-cause mortality

    Time frame: Up to 10 years After H. pylori eradication

    Korean National Health Insurance records or other reports

  6. Modification of atrophy score

    Time frame: Up to 10 years After H. pylori eradication

    Change in histologic atrophy grade from enrollment to subsequent endoscopic assessment

Sponsors and collaborators

Lead sponsor

National Cancer Center, Korea

Other Gov

Collaborators

  • Chonnam National University Hospital
  • Chuncheon Sacred Heart Hospital
  • Chung-Ang University Hospital
  • Incheon St.Mary's Hospital/The Catholic University
  • International Agency for Research on Cancer
  • Kangdong Sacred Heart Hospital
  • Kosin University Gospel Hospital
  • Kyungpook National University Hospital
  • Pusan National University Hospital
  • SMG-SNU Boramae Medical Center
  • Uijeongbu St. Mary's Hospital/The Catholic University

Registry information

Official study title

Effect of Helicobacter Pylori Eradication on Gastric Cancer Prevention in Korea: a Randomized Controlled Clinical Trial

Acronym: HELPER

Important dates

Study start
2014
Primary completion
2029
Study completion
2029
First posted
Apr 11, 2014
Registry last updated
Dec 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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