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Effect of cyclosporine oral myocardial injury in patients undergoing coronary artery bypass surgery hospital in Ahvaz Golestan second half of 2017: a randomized controlled clinical trial

Oral cyclosporine effect on myocardial damage heart

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017031533056N2
Enrollment
60
Registered
2017-06-21
Start date
2017-01-19
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

Myocardial heart. Myocardial degeneration

Interventions

Intervention 1: four to twelve hours before surgery given to patients cyclosporine capsules orally at a dose of 2.5 mg per kg for a single Dose under normal conditions and maitain general anesthesia
Treatment - Drugs
Four to twelve hours before surgery to patients given placebo orally All stages of operation under normal conditions and maintain general anesthesia and monitoring blood pressure and electrocardio
four to twelve hours before surgery given to patients cyclosporine capsules orally at a dose of 2.5 mg per kg for a single Dose under normal conditions and maitain general anesthesia and monitoring

Sponsors

Vice Chancellor for Research and Technology Development Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: - All patients who undergoing coronary artery bypass surgery . - Patients over 18 years - willingness to participate in the study Exclusion criteria - patients over 85 years - patients with unstable angina - Patients with moderate to severe renal impairment (glomerular filtration rate less than mL / min / m2 45) - developing cirrhosis of the liver - Oral administration of drugs glibenclamide or nicorandil (due to drug interactions).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Troponin_I. Timepoint: Troponin I measurements before surgery and at 24hr, 48hr and 72hr after surgery. Method of measurement: After preparing the evaluation kit little troponin (cTnI) by Golestan hospital laboratory.

Secondary

MeasureTime frame
CKMB. Timepoint: CKMB measurements before surgery and at 24hr, 48hr and 72hr after surgery. Method of measurement: CKMB measurements in the laboratory Golestan Hospital.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Mohammad hassan Adel

Ahwaz JundiShapur University of Medical Sciences

Dr.hassan.adel@gmail.com+98 61 3222 8037

Outcome results

None listed

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