Open vojtechhuser opened 4 years ago
We have patient level data.
Either the patient gave consent or we are using an exemption category.
Having an ethics expert (/IRB) on our team would be good.
Two modes:
I proposed the registry idea before. I would even want to lead such effort. File an official ClinicalTrials.gov virtual registry study.
Example is here: https://clinicaltrials.gov/ct2/show/NCT04302688
We have patient level data.
Either the patient gave consent or we are using an exemption category.
Having an ethics expert (/IRB) on our team would be good.
Two modes:
I proposed the registry idea before. I would even want to lead such effort. File an official ClinicalTrials.gov virtual registry study.
Example is here: https://clinicaltrials.gov/ct2/show/NCT04302688