Template to add a clinical trial

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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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Overview of Template to add a clinical trial

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Disease State(s) Studied (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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Ages

__ years to ___ years

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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Gender (Indicate whether men, women or both were enrolled)

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Study Sponsor (e.g. Investigator initiated or company name)

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Source of Data (Who is providing this data: publication, principal investigator, or co-investigator)

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Collaborators

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Investigators

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Oversight Authority (e.g. FDA, EMEA)

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Medline PMIDs

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External sites for further information (How to insert links)

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References (How to insert a reference)

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