Distributed Registry

Trial ID or NCT#

NCT03898570

Status

not recruiting iconNOT RECRUITING

Purpose

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.

Official Title

Distributed Registry Study

Eligibility Criteria

Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: Yes
Inclusion Criteria:
  1. 1. Patients with cardiovascular disease who are scheduled or have undergone either a) open or endovascular vascular procedure, or b) open or percutaneous cardiac procedure. 2. Patients with smartphones (iOS or Android) with unlimited data plans. 3. Patients who agree to remote surveillance
Exclusion Criteria:
  1. 1. Patients unwilling to download a research study app. 2. Data plans which are not unlimited.
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Investigator(s)

Oliver O. Aalami, MD
Vascular surgeon
Clinical Professor, Surgery - Vascular Surgery

Contact us to find out if this trial is right for you.

Contact

Doran S Triggs, BS
650-852-3459

View on ClinicalTrials.gov