Fact CheckerSign in

NCT07332494Not yet recruiting

Digital Remote Management for Care and Continuous Optimization Versus Usual Care in Patients With Coronary Heart Disease (DigiCare-CHD)

Source: ClinicalTrials.gov · Last updated 12 Jan 2026

Brief summary (registry, in English)

The DigiCare-CHD study is an investigator-initiated, multicenter, open-label, parallel-group randomized controlled trial. It aims to evaluated the efficacy of a smartphone-based digital remote management platform compared to usual care in achieving dual goal attainment of blood pressure and LDL-cholesterol levels in patients with coronary heart disease following percutaneous coronary intervention.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
792 (estimated)
First submitted
31 Dec 2025
Start date
Jan 2026
Primary completion date
Jul 2027
Lead sponsor
Beijing Anzhen Hospital
NCT number
NCT07332494

What you commit to

  • Study type: Interventional
  • Planned participants: 792
  • From Jan 2026 to the primary completion date, Jul 2027
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Severe sensory (hearing/vision) or cognitive impairment precluding device use
  • Conditions affecting adherence (e.g., substance use disorder, history of alcohol abuse)

Lab values

  • Heart Failure: NYHA Class III-IV or LVEF \< 40%.
  • Severe hepatic dysfunction (ALT/AST ≥3xULN or Total Bilirubin \>1.5 mg/dl)
  • Severe renal dysfunction (eGFR \< 30 ml/min/1.73m² or requiring dialysis)

Other

  • Uncontrolled hypothyroidism (TSH \>1.5xULN or \>10 mIU/L, or unstable dosage within 6 weeks)
  • Life expectancy \< 1 year due to non-cardiovascular comorbidities

Who the study is looking for

  • Age 18-75 years
  • Diagnosis of Acute Coronary Syndrome (ACS) or Chronic Coronary Syndrome (CCS)
  • Status post-successful percutaneous coronary intervention (PCI).
  • Possession of a smartphone and ability to operate the application (independently or with caregiver assistance).
  • Provision of written informed consent.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Beijing Tongren Hospital, Capital Medical University, Beijing, China
Coordinator of this site? Confirm its status
BeijingChinaUnknown status
13810720787
Coordinator of this site? Confirm its status
BeijingChinaUnknown status
The First Affiliated Hospital of Dalian Medical University, Dalian, China
Coordinator of this site? Confirm its status
DalianChinaUnknown status
The First Hospital of Jilin University, Changchun, China
Coordinator of this site? Confirm its status
Jilin CityChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.