VCT, ClinicalRSVP etc.

[bobwarnk]

Hey guys I’m new to clinical trials I actually just participated in my first one! I wanted to get some questions answered.

This whole deal with vct or any other subject registries is a thing I’d like to know more about.

How would I know if the site I used utilized one of these databases? Does it explicitly state so in the informed consent? My informed consent talked about deidentified codes being shared with The sponsor and their “partners” but didn’t specifically mention a registry. Is there any way to know?

[vark]

the sites that have vct have a seperate consent form for it. sometimes they scan your fingerprint right when you walk in. there's a thread that lists which places use it, no idea if it's up to date.

[labrat1]

A majority of topics on this site are not up to date