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The effect of perioperative Dexmedetomidine on renal function in patients undergoing CABG surgery and cardiopulmonary bypass

The effect of perioperative Dexmedetomidine on renal function in patients undergoing CABG surgery and cardiopulmonary bypass

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141009019470N83
Enrollment
60
Registered
2019-07-08
Start date
2019-07-11
Completion date
Unknown
Last updated
2019-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Bypass Grafting surgery and cardiopulmonary bypass. Atherosclerotic heart disease of native coronary artery

Interventions

Intervention 1: Intervention group: Patients in the dexmedmotidine group received doses of dexmedmotidine infusion at a dose of 0.5 micrograms / kg / h after induction of anesthesia until transmitted

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 70 Years

Inclusion criteria

Inclusion criteria: Age less than 70 years Patients undergoing coronary artery bypass graft surgery

Exclusion criteria

Exclusion criteria: Emergency Surgery Redo Surgery Performing a coronary artery bypass graft surgery with other cardiac surgery Preoperative renal problems and serum creatinine levels higher than 1.4 Ejection fraction less than 40% Known liver problems or high levels of liver enzymes Using balloon pump inside aorta.

Design outcomes

Primary

MeasureTime frame
Serum creatinine level. Timepoint: Before surgery, on the first, second and third days after surgery in ICU. Method of measurement: Blood sample.;Blood Urea Nitrogen. Timepoint: Before surgery, on the first, second and third days after surgery in ICU. Method of measurement: Blood sample.;Glomerular filtration rate. Timepoint: Before surgery, on the first, second and third days after surgery in ICU. Method of measurement: Cockcroft-Gault Equation Formula.

Secondary

MeasureTime frame
Inotropic Consumption in ICU. Timepoint: Before surgery, on the first, second and third days after surgery in ICU. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid Reza Lotfi

Shiraz University of Medical Sciences

hamidreza1368lotfi@gmail.com+98 51 3763 6108

Outcome results

None listed

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