Skip to content

Determining NAC mechanism in the prevention of early remodeling

Determining the mechanism of N-acetylcysteine in the prevention of early remodeling, role of oxidative stress

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201102283449N5
Enrollment
80
Registered
2011-08-01
Start date
2010-08-01
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 for 3 days per oral. Intervention 2: Control: Placebo BD for 3 days per oral.
Prevention
Intervention: NAC 600 mg BD for 3 days per oral
Control: Placebo BD for 3 days per oral

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria; Patients with criteria of first episode of ST-elevation AMI including typical chest pain with the duration of more than 30 minutes, >1-mm ST elevation in =2 adjacent limb leads or >2-mm ST elevation in =2 adjacent chest leads, and a raise in creatine kinase or in troponin T level 2 times the upper limit of normal were included in the study. Exclusion Criteria; Patients with history of prior AMI, heart failure, atrial fibrillation, valvular dysfunction, and neoplastic, renal, liver, or thyroid diseases were excluded from the study. Moreover patients with current acute or chronic infections, autoimmune diseases, surgical procedures in the past 3 months; under treatment with anti-inflammatory drugs, supplements and antioxidants, subsequent MI, discharge or death during the study period were excluded.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Tumor necrosis factor-alpha. Timepoint: 24 and 72 hours after administration of NAC or Placebo. Method of measurement: Elisa.;Transforming growth factor-beta. Timepoint: 24 and 72 hours after administration of NAC or Placebo. Method of measurement: Elisa.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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