Participate in our LATAM-SOLACI Peripheral Registries
Complete the following form and receive all the information and documentation needed to participate in the LATAM-SOLACI Peripheral Registry. If you wish to participate in the LATAM Bif-SOLACI Registry, please click on this link.
Complete the following form
Frequently Asked Questions
Who can participate in our LATAM-SOLACI Peripheral Registry?
All Latin American medical centers can participate.
Which cases can be registered in the LATAM-SOLACI Peripheral Registry?
Cases about patients with intermittent claudication and critical ischemia can be registered.
How does data collection work?
Patient information is collected using an electronic form designed with a unique personal access code within SOLACI’s REDcap platform.
What are the benefits of participating in the LATAM-SOLACI Peripheral Registry?
- Participants can consult our own database focused on lower limb angioplasty, with uniform variables for all Latin American centers.
- Participating centers can download, analyze, and publish their local data in real time, without requesting permissions or authorizations, thus creating collaborative knowledge.
- Researchers and centers participating in the registry can interact with other centers in the region looking to conduct research and publish papers.
- Researchers from the LATAM-SOLACI Peripheral Registry can credit their co-authorship of scientific articles and papers published using data from the Registry.
- Centers with high volume of registered patients in the LATAM-SOLACI Peripheral Registry can submit research proposals to be included in future papers.
- Researchers from the Registry can share the results of the LATAM-SOLACI Peripheral Registry in international and local events with previous authorization by SOLACI's Research Department.
- Should you need any assistance developing research projects or statistical analyzes, SOLACI's Research Department will provide help.
- SOLACI's Research Department will conduct continuous weekly audits so that all data are properly registered: both initial data and annual follow-ups (mandatory).