Skip to content

Impact of l-carnitine in percutaneous coronary intervention

Impact of L-carnitine on biomarkers of platelet activation in patients undergoing elective Percutaneous Coronary Intervention(PCI)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201212178698N4
Enrollment
80
Registered
2013-01-10
Start date
2012-12-30
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

ischemic heart disease. Myocardial ischemia followed by decreased oxygen to the myocardium

Interventions

Intervention 1: 3 gram L - carnitine is administrated to intervention patients one day before catheterization (1 g every 8 hours) and lasts for up to 24 hour after it (for two days). Patients blood s
Treatment - Drugs
3 gram L - carnitine is administrated to intervention patients one day before catheterization (1 g every 8 hours) and lasts for up to 24 hour after it (for two days). Patients blood sample is collect
Medication will not be given to patients in the control group. Patients blood sample is collected at baseline and 24 hour after catheterization.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:Patients with ischemic heart disease that have more than 50 percent occlusion in angiography findings and candidates for elective Pecrcutaneous Coronary Intevention.Exclusion criteria: cardiogenic shock;ST Elevation Myocardial Infarction;pregnant and lactating womens;patients under 18 years;immunologic or hematologic disorders;current infection;chronic kidney disease;serum creatinine above 2.5 mg/dl;hypothyroidism;epilepsy or convulsion;chronic liver disease;cancer

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Transforming growth factor beta(TGF-ß). Timepoint: baseline and 24 hour after. Method of measurement: Elisa kit.;CD40L. Timepoint: baseline and 24 hour after. Method of measurement: Elisa kit.;P-Selectin. Timepoint: baseline and 24 hour after. Method of measurement: Elisa kit.

Secondary

MeasureTime frame
Major adverse cardiac events)MACE). Timepoint: 1 month later. Method of measurement: evaluation of patient condition such as death, stent thrombosis confirmed by angiography ? acute coronary syndrome defined by AHA ? again revascularization with angioplasty or bypass.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzita Hajhossein Talasaz

Tehran University of Medical Sciences

atalasaz@razi.tums.ac.ir+98 21 6695 4709

Outcome results

None listed

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