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Comparison of prediction between TIMI (Thrombolysis in Myocardial Infarction) risk score and Modified TIMI risk score in discharged patients from emergency department with atypical chest pain

Comparison of prediction between TIMI (Thrombolysis in Myocardial Infarction) risk score and Modified TIMI risk score in discharged patients from emergency department with atypical chest pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201304182496N9
Enrollment
1000
Registered
2013-04-28
Start date
2011-06-19
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Atypical chest pain. Angina pectoris, unspecified

Interventions

Intervention 1: Group I was evaluated using TRS and its patients were discharged in case of having low risk (0-1). All criteria used in TRS method are of equal values and each score one. These criteri
Prevention
Group I was evaluated using TRS and its patients were discharged in case of having low risk (0-1). All criteria used in TRS method are of equal values and each score one. These criteria include: 1. i
Patients in group II were evaluated regarding their risk factors using MTRS method and were discharged in case of having low risk (0-1). The criteria used in MTRS system are similar to that of TRS. Th

Sponsors

Research Vice chancellor of Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients with chief complaints of atypical chest pain aged over 25 years old. Exclusion criteria: patients with the diagnosis of STEMI; patients younger than 25 years old; patients being hospitalized due to other reasons including dialysis requirements in CRF patients and myocardial contusion following chest trauma; pregnant women; imprisoned patients and unavailability of the follow-up for patients.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Atypical chest pain. Timepoint: on arrival and until 12 hours following symptoms onset. Method of measurement: ECGs and cardiac enzymes.

Secondary

MeasureTime frame
Adverse events. Timepoint: One month after admission in the emergency department. Method of measurement: All patients were followed up regarding the adverse events ((Myocardial Infarction (MI), revascularization and death)) and questionnaire form.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Hassan Soleimanpour

Tabriz University of Medical Sciences

h_mofid1357@yahoo.com+98 41 1335 2078

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026