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Study identifier: NCT06114615 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Recruiting

Digital Monitoring for Patients Post Coronary Interventions to Reduce Risk for Recurrent Adverse Cardiovascular Events

Condition: Coronary Artery Disease  ·  Sponsor: University of California, Davis

PhaseNA
Planned participants200
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

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About this study

The study aims to support patients immediately after percutaneous coronary intervention (PCI) by implementing a telemonitoring program. Eligible patients have coronary heart disease and undergo PCI. The intervention group receives remote monitoring and text-based follow-up, with established health goals and education on using the telemonitoring application, along with necessary devices. The control group gets standard care. Outcomes measured include blood pressure, LDL levels, patient satisfaction, revascularization, and mortality. The study findings will enhance patient care after PCI and contribute evidence for widespread telemonitoring implementation in healthcare systems, aiding medical therapy and lifestyle modifications.

This description comes directly from the study's public registry record.

Talk to the study team

Surabhi Atreja, MD  ·  (916) 734-2011  ·  smatreja@ucdavis.edu

Lina Du, BS

Always discuss trial participation with your own doctor first.

Locations (1)

University of California, Davis Medical Center Division of Cardiovascular MedicineSacramento, California, United StatesRecruiting

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