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Evaluation of the effect of Montelukast in patients with myocardial infarction

Evaluation of the effectivness of Montelukast on the hs-CRP level in patients with non ST-elevation myocardial infarction

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220516054874N4
Enrollment
68
Registered
2022-07-19
Start date
2022-08-06
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

Myocardial infarction with non-ST elevation. Non-ST elevation (NSTEMI) myocardial infarction

Interventions

Intervention 1: Intervention group: NSTEMI patients receiving montelukast 10 mg twice daily for one month along with standard treatment. Intervention 2: Control group: NSTEMI patients receiving placeb

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with non-ST-elevation MI according to the American College of Heart criteria Consent to admission to the study Age more than 18 years old No kidney failure under hemodialysis No kidney failure and GFR<30 No thrombocytopenia No severe liver failure with liver enzymes three times more than normal No treatment with corticosteroids or immunosuppressive drugs No treatment with diltiazem or verapamil No history or prone to suicide No previous treatment with Montelukast

Exclusion criteria

Exclusion criteria: Lack of consent to continue the study

Design outcomes

Primary

MeasureTime frame
Changes in hs-CRP serum level. Timepoint: At the beginning of the study and after 4 weeks of treatment. Method of measurement: Laboratory kit.

Secondary

MeasureTime frame
Changes in CBC diff. Timepoint: At the beginning of the study and after 4 weeks of treatment. Method of measurement: Laboratory kit.;Changes in lipid profile. Timepoint: At the beginning of the study and after 4 weeks of treatment. Method of measurement: Laboratory kit.;Changes in Interleukin-6 levels. Timepoint: At the beginning of the study and after 4 weeks of treatment. Method of measurement: Laboratory kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Vafa Baradaran Rahimi

Mashhad University of Medical Sciences

baradaranrv@mums.ac.ir0095 5138012739

Outcome results

None listed

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