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The Evaluation of the ST Segment Using the Automatic Monitoring Function

The Evaluation of the ST Segment Using the Automatic Monitoring Function - ESTIMATION

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000011824
Enrollment
450
Registered
2013-09-20
Start date
2011-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Ischemic Cardiac Disease

Interventions

None listed

Sponsors

Associations for Establishment of Evidence in Interventions (AEEI)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patients who have been implanted or have scheduled to implant ICD attached with ST monitoring function 2. The patients with a previous history of ischemic cardiac disease

Exclusion criteria

Exclusion criteria: 1. The patients who is complete atrioventricular block (the patients who will implant atrial pacing definitely). 2. Under age 20. 3. Patients who are considered inappropriate for enrollment in this study, such as patients who cannot follow clinical research enough (limited life expectancy, mental disorder) 4. The patients who Brugada syndrome.

Design outcomes

Primary

MeasureTime frame
1. To observe continuous ST changes by intracardiac Electrogram (EGM) and to investigate the effectiveness of setting the recommendation value. 2. To investigate the involvement of myocardial ischemia in the episode of ventricular tachycardia and ventricular fibrillation 3. To investigate that shock therapy triggers the exacerbation of myocardial ischemia or the cause of myocardial disorder.

Countries

Japan

Contacts

Public ContactHiroki Takayama

Soiken Inc. Division of Clinical Study Support

takayama@soiken.com03-3295-1376

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026