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Effect of Aortic Root Infusion of Sufentanil on Ischemia-Reperfusion Injury in Patients Undergoing Coronary Artery Bypass

Effect of Aortic Root Infusion of Sufentanil on Ischemia-Reperfusion Injury in Patients Undergoing Coronary Artery Bypass

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017080619470N62
Enrollment
60
Registered
2017-10-24
Start date
2017-12-22
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

Coronary Artery Bypass Surgery. Atherosclerotic heart disease

Interventions

Intervention 1: 1 µg/kg sufentanil is injected in post-conditioning group through the cardiopulmonary cannula 5 minutes before Cross Clamp and then cold blood cardioplegia solution with antigrad metho
Treatment - Drugs
1 µg/kg sufentanil is injected in post-conditioning group through the cardiopulmonary cannula 5 minutes before Cross Clamp and then cold blood cardioplegia solution with antigrad method will be inject
In the control group, patients receive 5 cc normal saline through the cardiopulmonary cannula 5 minutes before Cross Clamp and then cold blood cardioplegia solution with antigrad method will be inje

Sponsors

Vice Chancellor for Research, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria :20-65-year-old adults undergoing elective CABG. Exclusion criteria: History of preceding arrhythmia; Ejection fraction less than 35%; recent myocardial infarction (less than 6 months); renal or liver failure; permanent or temporary pacemaker; hypertension; AV block or bradycardia less than 50 heart beat In minutes; congestive heart failure (CHF); re-operation; history of diabetes.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The serum level of CPK-MB enzymes, troponin I. Timepoint: at the induction of anesthesia 6, 12, and 24 hours after surgery. Method of measurement: Arterial blood sample.;Inotropic scores criteria. Timepoint: After arrival to the ICU and inthe operating room. Method of measurement: Observasion.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Tahari

Shiraz University of Medical Sciences

taharimehdi@yahoo.com+98 71 3647 4270

Outcome results

None listed

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