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A Prognostic Marker in Acute Coronary Syndrome

De Ritis Ratio (AST/ALT) As A Prognostic Marker in Acute Coronary Syndrome - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/05/087648
Enrollment
92
Registered
2025-05-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: I219- Acute myocardial infarction, unspecified

Interventions

Intervention1: Nil: Nil

Sponsors

Datta Meghe Institute of Medical Sciences Sawangi Meghe Wardha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: PATIENTS WHO HAVE SYMPTOMS AND CONFIRMED ACUTE MYOCARDIAL INFARCTION. PATIENTS WHO ARE DIAGNOSED IN ACCORDANCE WITH CARDIAC BIOMARKERS SUCH AS TROPONIN-I AND ELECTROCARDIOGRAM. PATIENTS WHO CONSENTED FOR BEING INCLUDED IN THE STUDY.

Exclusion criteria

Exclusion criteria: RENAL FAILURE, CANCER, ACUTE PANCREATITIS. LIVER DISEASES. CONGESTIVE CARDIAC FAILURE STROKE ANY ACUTE RESPIRATORY EMERGENCY PRESENCE OF IMMUNE SYSTEM DISEASES, MALIGNANT TUMOR, HEMATOLOGICAL DISEASES. ANEMIA. PREGNANCY.

Design outcomes

Primary

MeasureTime frame
If de Ritis ratio (AST/ALT) 2.0 then higher is the severity of acute coronary syndromeTimepoint: At the time of the admission and mid of the treatment.—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactShaikh Suhail Shaikh Maqbool

Datta Meghe Institute of Higher Education and Research

anujvarma1985@gmail.com8623917888

Outcome results

None listed

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