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Updated: Jan 22, 2026

In Silico Clinical Trials for Cardiovascular Disease
Published on: May 27, 2022
Ensuring trial conduct is consistent with trial design: assumption is the enemy of quality
Joanna Kelly1, Barry Hounsome2, Gill Lambert2
1Kings College London Clinical Trials Unit, Research Management and Innovation Directorate, King's College London, M2.06, 16 De Crespigny Park, London, SE5 8AF, UK. joanna.kelly@kcl.ac.uk.
Abstract:
'Assumptions are made and most assumptions are wrong' (Albert Einstein) Clinical trial conduct must be consistent with trial design, yet conducting the trial according to plan remains a major challenge.We discuss the importance of optimal co-applicant team formation in trial leadership, appropriate delegation of tasks and staff supervision arrangements. Finally, we discuss five standard documents which we believe require particular attention. With appropriate engagement by or with co-applicants during the preparation of these five standard documents, we believe many of the pitfalls trials commonly experience can be avoided. The risks inherent in failing to identify and address mistaken assumptions during the preparation of these documents are discussed and recommendations for best practice suggested.
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