Azithromycin And Coronary Events Study In Patients With Stable Coronary Disease
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Complete Title of Study
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Study Acronym (The trial's abbreviation if there is one)
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Principal Investigator, Co-investigators, and Collaborating Institutions
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Overview of Trial
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Disease State(s) Studied (e.g. acute MI, breast cancer, etc.)
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Study Phase (e.g. Phase I,II,III,IV) Study Phases are defined here
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Study Design (e.g. multicenter, randomized, double blind, placebo controlled)
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Study Arms and How They Were Treated (Intervention) (Explanation here)
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Primary Pre-Specified Endpoint
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Secondary Endpoints
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Inclusion Criteria
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Exclusion Criteria
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Outcome: Primary endpoint (Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)
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Outcome: Secondary endpoint (Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)
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Outcome: Exploratory endpoints (Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)
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Outcome: Safety endpoints (Report both relative risk and absolute risk as well as number needed to harm if available)
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Conclusions of the Investigators (Quote the investigators conclusions here)
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Commentary, Discussion and Limitations of the Trial (Anyone can add comments)
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Slides
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Video Commentary
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References (How to insert a reference)
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External sites for further information (How to insert links)
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Detailed information about the trial
Ages
__ years to ___ years
Gender (Indicate whether men, women or both were enrolled)
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Accepts Healthy Volunteers (Answer yes or no)
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Enrollment Period (Study start and end date)
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Recruitment Status (explanation)
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Enrollment (Total number of patients enrolled)
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Study Sponsor (e.g. Investigator initiated or company name)
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Source of Data (Where is this data on this page coming from: publication, principal investigator, or co-investigator)
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