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Clinical Trials in China / NCT03629418
Recruiting Not applicable

Targeted Blood-pressure Management and Acute Kidney Injury After Coronary Artery Bypass Surgery

NCT03629418 · tracked via the Priya Life Science China tracker
Sponsor
Peking University First Hospital
Phase
Not applicable
Started
2018-08-14
Last updated
2025-07-30

Condition(s) studied

Coronary Artery Bypass, Off-PumpIntraoperative HypotensionAcute Kidney InjuryPreventive MedicineIntraoperative Care

Investigational drug(s) / intervention(s)

Targeted blood-pressure management →Routine blood-pressure management

Targeted blood-pressure management: Prophylactic norepinephrine infusion is started before anesthetic induction and maintained throughout surgery. The target is to maintain systolic blood pressure at 110 mmHg or higher.

Routine blood-pressure management: Phenylephrine (25-50 ug) is injected or vasopressors is infused only when necessary. The target is to maintain systolic blood pressure at 90 mmHg or higher during surgery.

Study summary

Acute renal injury (AKI) is a common complication after cardiac surgery and is associated with worse outcomes. It is now realized that intraoperative hypotension is an important risk factor for the development of AKI. In a recent randomized controlled trial of patients undergoing major noncardiac surgery, intraoperative individualized blood-pressure management reduced the incidence of postoperative organ dysfunction. The investigators hypothesize that, for patients undergoing off-pump CABG, targeted blood-pressure management during surgery may also reduce the incidence of postoperative AKI.

Eligibility

Sex
ALL
Min age
50 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 50 years; * Scheduled to undergo off-pump CABG surgery. Exclusion Criteria: * Refuse to participate; * Untreated or uncontrolled severe hypertension (systolic blood pressure ≥180 mmHg or diastolic blood pressure ≥110 mmHg); * Chronic kidney disease with a glomerular filtration rate \< 30 ml/min/1.73 m2 or end-stage renal disease requiring renal-replacement therapy; * Inability to communicate during the preoperative period because of coma, profound dementia, language barrier, or end-stage disease; * Requirement of vasopressors/inotropics to maintain blood pressure before surgery; * Second or emergency surgery; * Expected survival of less than 24 hours.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beijing University First Hospital Beijing Beijing Municipality Recruiting

More Peking University First Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03629418 on ClinicalTrials.gov ↗ ← All trials in China