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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ISRCTN |
Last refreshed on:
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5 June 2018 |
Main ID: |
ISRCTN40431563 |
Date of registration:
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04/05/2018 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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New mobile application reduces the time lost in patients with a heart attack
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Scientific title:
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Significant benefits of new communication technology for time delay management in STEMI patients. |
Date of first enrolment:
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01/08/2016 |
Target sample size:
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220 |
Recruitment status: |
Completed |
URL:
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http://isrctn.com/ISRCTN40431563 |
Study type:
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Observational |
Study design:
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Longitudinal case series observational single centre study (Treatment)
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Phase:
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Countries of recruitment
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Slovakia
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Contacts
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Name:
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Martin
Studencan |
Address:
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Teaching Hospital of J.A.Reiman
Cardiology Clinic
Holleho 14
08001
Presov
Slovakia |
Telephone:
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Email:
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: 1. Adult age 45 - 86 2. Suffering from chest pain 3. Visited by EMS staff once ECG has been recorded and suspicion raised about STEMI
Exclusion criteria: No specified exclusion criteria.
Age minimum:
Age maximum:
Gender:
Both
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Health Condition(s) or Problem(s) studied
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ST-elevation myocardial infarction (STEMI) Circulatory System ST-elevation myocardial infarction (STEMI)
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Intervention(s)
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Paramedics in the field spend 2 months responding to chest pain calls using no remote ECG evaluation and medical treatment as normal. They then spend 5 months responding to calls of chest pain, using smartphone technology to communicate with specialists in the local cardiocentre, aiming to evaluate the ECG and establish a diagnosis of STEMI remotely. If this is confirmed, they arrange primary transportation of the patient to the cathlab.
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Primary Outcome(s)
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1. Total ischemic period measured using time interval between symptom onset (according to the patient, stated in medical records) and time of PCI procedure (moment of PCI wire insertion) stated in medical records by cardiologist performing the procedure. 2. Proportion of unwanted secondary transportation calculated using information from medical records. The number of STEMI patients transported to the cardiocentre by EMS via secondary transportations is compared to the number of all STEMI patients.
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Secondary Outcome(s)
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Technological reliability of the communication technology is assessed by measurement of an ECG transmission time. If the transmission fails or if it overcame 3 minutes – it is considered to be unsuccessful. Transmission within 3 minutes is considered to be successful.
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Secondary ID(s)
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appSTEMI trial
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Source(s) of Monetary Support
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Presov University
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Ethics review
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Status:
Approval date:
Contact:
Ethics approval not required: retrospective observational study, only anonymous data analysis and reporting. No medication but standard medical care was applied. Use of new communication technology has been used.
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Results
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Results available:
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Yes |
Date Posted:
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Date Completed:
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12/09/2017 |
URL:
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