3NANC: Prevention of Recurrent Ulcer Bleeding in High-risk Aspirin Users Who Are Not Infected With Helicobacter Pylori

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Completed
CT.gov ID
NCT01274767
Collaborator
(none)
467
1
188
2.5

Study Details

Study Description

Brief Summary

Low-dose aspirin is the mainstay of treatment for patients with coronary heart disease and stroke. However, low-dose aspirin increases the risk of ulcer bleeding. Current evidence indicates that 80 - 100 mg of aspirin daily provides good protection against vascular events and the risk of ulcer bleeding is low (about 1% per year). Since the overall risk of bleeding is low, aspirin users who do not have previous ulcer disease do not require prophylaxis with anti-ulcer drugs. In contrast, aspirin users with a history of ulcer disease have a 2- to 4-fold increased risk of ulcer bleeding. The best strategy for reducing the risk of bleeding in high-risk aspirin users remains unclear. Current strategies for high-risk patients include the use of anti-ulcer drugs, elimination of risk factors (e.g. Helicobacter pylori), or the use of enteric-coated aspirin.

Although co-therapy of aspirin with an acid suppressant reduces the risk of ulcer bleeding, drug compliance may limit its clinical usefulness particularly in patients who are already receiving multiple drugs. The efficacy of enteric-coated aspirin in preventing ulcer complications showed conflicting results. One study found that enteric-coated aspirin increases the risk of ulcer bleeding. A recent study showed that enteric-coated aspirin causes minimal acute gastric injury.

The investigators postulated that among patients without H. pylori infection and a history of ulcer bleeding who continue to use low-dose aspirin, enteric-coated aspirin reduces the long-term risk of ulcer complications to a level that is comparable to that of average-risk aspirin users.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Low-dose aspirin is increasingly used for the prophylaxis against coronary heart disease and stroke. However, it is also an important cause of peptic ulcer bleeding worldwide. In England and Wales, low-dose aspirin is estimated to account for about 10% of ulcer bleeding in people aged 60 and over [Weil 1995]. The problem of aspirin-related ulcer disease is expanding with the increasing use of aspirin for cardiovascular prophylaxis.

    No dose of aspirin is entirely free of risk. Using a daily dose of aspirin as low as 75 mg, the risk of ulcer bleeding doubles that of non-users [Weil 1995]. Previous ulcer disease and concurrent major medical illnesses are important risk factors for ulcer bleeding with low-dose aspirin. Among aspirin users, those with previous ulcer disease have a 5-fold increased risk of ulcer bleeding [Lanas 2000].

    Various strategies have been used to prevent recurrent ulcer bleeding in high-risk aspirin users, such as eradication of Helicobacter pylori, the use of prophylactic anti-ulcer drugs or enteric-coated aspirin. Recently, the investigators have shown that the eradication of H. pylori is comparable to maintenance treatment with omeprazole, a potent acid suppressant, in preventing recurrent ulcer bleeding for high-risk aspirin users [Chan 2001]. However, about 50% of aspirin users are not infected with H. pylori.

    The optimal strategy to prevent ulcer complications for high-risk aspirin users who are not infected with H. pylori remains undefined. Although co-therapy of aspirin with an acid suppressant reduces the risk of ulcer bleeding, drug compliance may limit its clinical usefulness particularly in patients who are already receiving multiple drugs.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    467 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Prevention of Recurrent Ulcer Bleeding in High-risk Aspirin Users Who Are Not Infected With Helicobacter Pylori: A Prospective Cohort Study (NSAID#3NANC Study)
    Study Start Date :
    Jan 1, 1995
    Actual Primary Completion Date :
    Jun 1, 2010
    Actual Study Completion Date :
    Sep 1, 2010

    Arms and Interventions

    Arm Intervention/Treatment
    High risk cohort

    Patients having history of endoscopically confirmed ulcer bleeding, need long-term aspirin for cardiovascular or cerebrovascular prophylaxis and have a negative test for H. pylori based on histology

    Average risk cohort

    Patients having no history of endoscopically confirmed ulcer bleeding, need long-term aspirin for cardiovascular or cerebrovascular prophylaxis and have H. pylori positive OR negative

    Outcome Measures

    Primary Outcome Measures

    1. Ulcer complications [10 years]

      defined as bleeding or perforation

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    High risk cohort:
    Inclusion Criteria:
    1. History of endoscopically confirmed ulcer bleeding

    2. Need long-term aspirin for cardiovascular or cerebrovascular prophylaxis

    3. A negative test for H. pylori based on histology

    Exclusion Criteria:
    1. Concomitant use of anti-ulcer drug, anticoagulant, non-aspirin NSAIDs or steroids

    2. Current or past H. pylori infection

    3. Previous acid-reduction gastric surgery

    4. Gastric outlet obstruction, erosive esophagitis, gastroesophageal varices

    5. Moribund or incurable cancers

    Average-risk cohort

    Inclusion criteria:
    Patients must fulfill ALL of the following:
    1. No history of ulcer bleeding

    2. Need long-term aspirin for cardiovascular or cerebrovascular prophylaxis

      1. pylori positive OR negative
    Exclusion criteria:
    1. Concomitant use of anti-ulcer drug, anticoagulant, non-aspirin NSAIDs or steroid

    2. Previous acid-reduction gastric surgery

    3. Moribund or incurable cancers

    4. Previous attempts of H. pylori eradication

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Prince of Wales Hospital Hong Kong China

    Sponsors and Collaborators

    • Chinese University of Hong Kong

    Investigators

    • Principal Investigator: Francis KL CHAN, MD, Chinese University of Hong Kong

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Francis KL Chan, Professor, Chinese University of Hong Kong
    ClinicalTrials.gov Identifier:
    NCT01274767
    Other Study ID Numbers:
    • 3NANC
    First Posted:
    Jan 12, 2011
    Last Update Posted:
    Apr 24, 2017
    Last Verified:
    Apr 1, 2017
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 24, 2017