After the SYNTHESIS and IMS-3 trials, what population should this be attempted in? Certainly not all comers. In addition, newer devices seem to lead to faster recanalization, therefore can newer devices, used in appropriately selected early patients, improve outcomes versus legitimate maximal medical management (without crossover's) in a randomized trial.
I think the use of the new devices over the old ones, since the are increased reperfusion rates with endovascular procedures but for instance, the IMS-III didn't have many new devices before the trial was stopped i.e. the new stent retriever technology.