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Evaluation of N-acetylcystein effects on cardiac remodeling biomarkers

Evaluating the effect of N-acetyl cysteine on the Early Remodeling Biomarkers (MMPs & NT-Pro-BNP) in patients following acute myocardial infarction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138905093449N2
Enrollment
100
Registered
2010-09-04
Start date
2010-08-23
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

Acute Myocardial Infarction. Acute myocardial infarction

Interventions

Intervention 1: Intervention: NAC 600 mg BD PO for 3 days. Intervention 2: Control: Placebo BD PO for 3 days.
Prevention
Intervention: NAC 600 mg BD PO for 3 days
Control: Placebo BD PO for 3 days

Sponsors

Tehran University of Medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: ST-elevation AMI diagnosed by the following criteria: (1) typical chest pain lasting >30 minutes, (2) 1-mm ST elevation in 2 contiguous limb leads or 2-mm ST elevation in 2 contiguous chest leads, and (3) increase in creatine kinase or in troponin T level to 2 times the upper limit of normal. Exclusion criteria: previous AMI or HF, AF or valve disease, and history of neoplastic, renal, liver, or thyroid disease, acute or chronic infections or autoimmune diseases, under treatment with anti-inflammatory drugs, or underwent surgical procedures in the preceding 3 months, unwillingness for entering in the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
MMP-9 as early cardiac remodeling biomarker. Timepoint: 24 and 72 hours after administration of NAC. Method of measurement: Elisa.;Nt-pro-BNP as early cardiac remodeling biomarker. Timepoint: 24 and 72 hours after administration of NAC. Method of measurement: Elisa.;MMP-2 as early cardiac remodeling biomarker. Timepoint: 24 and 72 hours after administration of NAC. Method of measurement: Elisa.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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