WIN is considering developing a data registry exclusive to female TAVR patients. The goal is to ensure meaningful data through the inclusion of appropriate data fields. The data will be used for future study and queries regarding TAVR as WIN continues on its mission to improve patient care.
If your institution might be interested in participating in a European TAVR registry exclusively for female patients, please complete the very brief 5-question survey below. Additionally, if you know of other European centers that might be interested in participating, please pass this survey link on to them. Once WIN has determined if such a registry would be successful, institutions will be recruited to participate in the project.