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Telemedicine Follow-up for Post-ACS Patients

Telemedicine Follow-up for Post-Acute Coronary Syndrome Patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04485754
Enrollment
88
Registered
2020-07-24
Start date
2020-05-15
Completion date
2021-12-31
Last updated
2026-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ACS - Acute Coronary Syndrome

Keywords

Telemedicine follow-up visit, Post-ACS rehabilitation

Brief summary

The aim is to compare the safety of using telemedicine and office visit follow-up in post-acute coronary syndrome patients

Detailed description

Rehabilitation after acute coronary syndrome includes visits to the cardiologist's office at 1, 2, 6 and 12 months after discharge. Due to the Covid-19 pandemic, visiting a cardiologist's office maybe impossible. In such cases telemedicine follow-up visit would be reasonable choice. Taking into account the absence of studies in this area, providing investigation evaluating parameters of safety for both methodics is relevant.

Interventions

OTHERTelemedicine FU

Participant will get telemedicine follow-up visit at 1, 3, and 6 months or 1 and 6 months after discharge from hospital.

OTHEROffice FU

Participant will get office follow-up visit at 1, 3, and 6 months or 1 and 6 months after discharge from hospital.

Sponsors

Tomsk National Research Medical Center of the Russian Academy of Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Signed informed consent 2. Age ≥ 40 years 3. PCI with coronary artery stenting for ACS 4. Angiographic success PCI

Exclusion criteria

1. Patients with cancer 2. Severe CHF (EF LV \<35% or functional class of heart failure III-IV NYHA) 3. Severe valvular heart disease or Prosthetic heart valves. 4. Severe forms of CKD (GFR\<30mL/min) 5. Planned staged revascularization during the next 12 months 6. Planned surgery within the next 12 months

Design outcomes

Primary

MeasureTime frameDescription
MACCE1 yearMajor adverse cardiac and cerebrovascular events: cardiac death, myocardial infarction, or stroke

Secondary

MeasureTime frameDescription
High level of MT optimization1 yearHigh Level of Medical Therapy Optimization is defined as a participant meeting all of the following goals: LDL \< 1.4 mmol/L and on any statin, blood pressure \< 140/90 mm/Hg (\<135/85 mm/Hg for patients with diabetes mellitus), on aspirin or other antiplatelet or anticoagulant, and not smoking. High level of medical therapy optimization is missing if any of the individual goals are missing.
PB < 140/90 mm/Hg (<135/85 mm/Hg for Diabetes)1 yearBlood pressure \< 140 mm/Hg (\<135/85 mm/Hg for for patients with diabetes mellitus)
LDL < 1.4 mmol/L1 yearLow density lipoprotein\< 1.4 mmol/L
Not smoking1 yearNot smoking
Decrease in overweight1 yearDecrease in overweight
Aspirin or other antiplatelet or anticoagulant1 yearAdherence to aspirin or other antiplatelet or anticoagulant
Adherence to prescribed medication1 yearAdherence to prescribed at discharge medication
Hospitalization1 yearHospitalization for cardiac reasons

Countries

Russia

Contacts

PRINCIPAL_INVESTIGATORIvan S Bessonov, MD, PhD

Tyumen Cardiology Research Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 25, 2026