NCT07049302View on ClinicalTrials.gov

Comparison of Conventional and Non-Conventional CRF and Their Association With Acute Coronary Syndrome

Active, not recruitingOBSERVATIONAL
Enrollment

222

Participants

Timeline

Start Date

March 17, 2025

Primary Completion Date

September 1, 2025

Study Completion Date

February 28, 2026

Conditions
Coronary Syndrome
Interventions
COMBINATION_PRODUCT

Conventional Risk Factor Assessment

Participants in Group 1 will undergo evaluation for conventional cardiovascular risk factors associated with Acute Coronary Syndrome (ACS

COMBINATION_PRODUCT

Non-Conventional Risk Factor

Participants in Group 2 will be assessed for non-conventional cardiovascular risk factors associated with Acute Coronary Syndrome (ACS).

Trial Locations (1)

Unknown

Tertiary care hospital, Peshawar

All Listed Sponsors
lead

Superior University

OTHER