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Telemedicine Follow-up for Post-ACS Patients

T

Tomsk National Research Medical Center of the Russian Academy of Sciences

Status

Completed

Conditions

ACS - Acute Coronary Syndrome

Treatments

Other: Telemedicine FU
Other: Office FU

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Full 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.

Enrollment

88 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

88 participants in 2 patient groups

Telemedicine FU
Experimental group
Description:
Telemedicine follow-up visit at 1, 3, and 6 months or 1 and 6 months after discharge from hospital.
Treatment:
Other: Telemedicine FU
Office FU
Active Comparator group
Description:
Office follow-up visit at 1, 3, and 6 months or 1 and 6 months after discharge from hospital.
Treatment:
Other: Office FU

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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