Abstract
A simple framework for assessing and reporting data availability in an ongoing clinical trial is described. Protocol requirements, visit schedules and data availability are combined into a simple report to track the progress of a study.
Publication types
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Letter
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Research Support, N.I.H., Extramural
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Anti-Retroviral Agents
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Clinical Trials Data Monitoring Committees*
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Clinical Trials as Topic / methods*
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HIV Infections* / drug therapy
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Humans
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Research Design*
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Research Subjects
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Time Factors