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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00251966
Registration number
NCT00251966
Ethics application status
Date submitted
9/11/2005
Date registered
11/11/2005
Date last updated
12/03/2009
Titles & IDs
Public title
ASTERIX: Low Dose ASA and Nexium
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Scientific title
A Randomized Double-Blind Placebo-Controlled Study to Assess the Prevention of Low-Dose Acetylsalicylic Acid (ASA) Associated Gastroduodenal Lesions and Upper Gastrointestinal Symptoms in Patients Taking Esomeprazole 20 mg Once Daily for 26 Weeks.
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Secondary ID [1]
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D9617C00011
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Gastroesophageal Reflux
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Condition category
Condition code
Oral and Gastrointestinal
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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The primary variable is presence of gastric and/or duodenal ulcers at endoscopy over a 26-week period in patients taking low-dose ASA.
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Assessment method [1]
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Timepoint [1]
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Secondary outcome [1]
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LA classification for the oesophagus at endoscopy. Upper GI symptoms assessed by the investigator at each study visit.
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Assessment method [1]
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Timepoint [1]
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Eligibility
Key inclusion criteria
* A clinical diagnosis of a condition (cardiovascular and/or cerebrovascular protection or other reasons) that requires daily intake of low-dose ASA, 75-325 mg, and is expected to continue for the duration of the study (daily is defined as at least 5 days per week).
* Age >= 60 years.
* No gastric and/or duodenal ulcer at the baseline endoscopy.
* H. pylori negative by serology test at screening.
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Minimum age
60
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Upper GI symptoms
* Erosive oesophagitis
* Malignancy
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/05/2004
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/09/2005
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Sample size
Target
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC
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Recruitment hospital [1]
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Research Site - Bondi Junction
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Research Site - Bracken Ridge
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Research Site - Carina Heights
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Research Site - Adelaide
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Research Site - Ashford
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Research Site - Wayville
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Research Site - Woodville
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Research Site - Ballarat
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Recruitment hospital [9]
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Research Site - Malvern
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Recruitment postcode(s) [1]
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- Bondi Junction
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Recruitment postcode(s) [2]
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- Bracken Ridge
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- Carina Heights
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- Adelaide
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- Ashford
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- Wayville
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- Woodville
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- Ballarat
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Recruitment postcode(s) [9]
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- Malvern
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Recruitment outside Australia
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Bulgaria
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Burgas
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Bulgaria
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Pleven
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Edinburgh
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
AstraZeneca
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of the study is to evaluate the effect of esomeprazole 20 mg od versus placebo for the prevention of gastric and/or duodenal ulcers in patients taking low-dose ASA.
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Trial website
https://clinicaltrials.gov/study/NCT00251966
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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AstraZeneca Nexium Medical Science Director, MD
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Address
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AstraZeneca
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00251966
Download to PDF