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Clinical Trial Summary

The purpose of this study is to test if a patient can be directly connected to a quality assurance (QA) database, traditionally known as a registry. Patient-reported outcomes (PRO) data will be entered into the database directly from a patient's mobile phone from their index procedure for 12 months. The investigators hope this study to be a "proof of concept" for such a distributed registry and evaluate 1) consistency of data acquisition, 2) engagement of patients, 3) overall value of patient-reported outcomes to enhance long term follow up.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03898570
Study type Observational [Patient Registry]
Source Stanford University
Contact
Status Completed
Phase
Start date April 1, 2019
Completion date March 1, 2021

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