Dr T didn’t say there were no interdependencies or delays. It was @ma420 that stated this here.
I do think DrT’s response was unintentionally ambiguous. “Data” in the context of his response would have been final readouts.
“Data” for the purpose of trial design is perhaps interim analysis based on a smaller number of patients. I don’t think they would need data from all 50 patients to get a “feel” for parameters to use to
design the cardioprotection trial.
Also recognise that recruitment criteria for the observational study is fairly narrow … two or more cardiac risk factors. This means that all of the patients recruited into the observational study will generate data that can contribute in some way to trial design ( once analysed for say the first dozen or so patients ).
Dr T didn’t say there were no interdependencies or delays. It...
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