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Effect of Remote Ischemic Preconditioning on the Incidence of Acute Kidney Injury in Patients Undergoing Coronary Artery Bypass Graft Surgery

Effect of Remote Ischemic Preconditioning on the Incidence of Acute Kidney Injury in Patients Undergoing Coronary Artery Bypass Graft Surgery: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017110537254N1
Enrollment
180
Registered
2017-11-09
Start date
2013-11-02
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

Condition 1: Acute kidney injury. Condition 2: Remote ischemic preconditioning. Condition 3: Coronary artery bypass graft surgery.

Interventions

Intervention 1: Intervention: RIPC Patients in the remote ischemic preconditioning (RIPC) group will receive three sequential sphygmomanometer cuff inflations on their right upper arm after induction
Prevention
Placebo
Intervention: RIPC Patients in the remote ischemic preconditioning (RIPC) group will receive three sequential sphygmomanometer cuff inflations on their right upper arm after induction of anesthesia i
Control: sham-RIPC Patients in the sham-RIPC group will have the sphygmomanometer cuff placed on their right upper arm, but the cuff will not be inflated. Similar to patients in the RIPC group, patie

Sponsors

Vice chancellery for research affairs, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: • Candidate cardiac surgical patients • Elective or urgent on pump coronary artery bypass grafting (CABG) • Age 18 to 85 years • Signed informed consent Exclusion Criteria: • End-stage renal disease (receiving hemodialysis or glomerular filtration rate <15 ml/min/1.73m2) • Peripheral vascular disease • Severe hepatic disease • Planned off-pump surgery • Pregnancy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative acute kidney injury (AKI). Timepoint: Within the first 72 hours after surgery. Method of measurement: Defined as an elevation of serum creatinine of =0.3 mg/dl or =50% within 72 hours after surgery.

Secondary

MeasureTime frame
Duration of hospital stay. Timepoint: Through hospital stay after surgery. Method of measurement: in days.;Duration of ICU stay. Timepoint: Through ICU stay. Method of measurement: in days.;All cause mortality. Timepoint: Through hospital stay after surgery. Method of measurement: number of observed cases.;Requiring hemodialysis. Timepoint: Through hospital stay after surgery. Method of measurement: number of observed cases.;Postoperative liver function. Timepoint: Preoperatively and at 24 h post-surgery. Method of measurement: By measuring serum AST, ALT, T.bilirubin, and albumin.;Incidence of postoperative atrial fibrillation (AF). Timepoint: Within the first 72 hours after surgery. Method of measurement: Defined as the incidence of new-onset AF lasting for five minutes or longer.;Incidence of postoperative stroke. Timepoint: Through hospital stay after surgery. Method of measurement: Defined as a new ischemic or hemorrhagic cerebrovascular accident with neurological deficit lasting >24 h.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSina Bagheri

Shiraz nephro-urology research center

bagherisi@sums.ac.ir+98 71326281563

Outcome results

None listed

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