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Impact of perioperative vasopresin use on postoperative atrial fibrillation in cardiovascular surgery

Impact of perioperative vasopresin use on postoperative atrial fibrillation in cardiovascular surgery - VASOAF study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs041230034
Enrollment
184
Registered
2023-06-09
Start date
2024-03-14
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Coronary artery disease, aortic disease and aortic valve disease in adult Coronary Artery Disease, Aortic Diseases, Aortic Valve Disease

Interventions

After aortic cross clamp, we will start to infusion trial or placebo drugs at 1.5 mL/hour.Targeted mean arterial pressure is 60 mmHg at arterial line monitoring or non invasive blood pressure. 1 bloo
Randomized Controlled Trial

Sponsors

Akiyama Koichi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Male and Female Age 18 years old to 85 years old weight 40kg to 120kg Patients underwent cardiovascular surgery with cardiopulmonary bypass Understand the research and obtain written consent

Exclusion criteria

Exclusion criteria: Chronic or paroximal atrial fibrillation mitral valve surgery minimally invasive cardiac surgery non median sternotomy hyponatremia Chronic kidney disease on hemodialysis Patients who is not eligible for candidate for trial

Design outcomes

Primary

MeasureTime frame
Primary Outcome is rate of post operative atrial fibrillation within 3 days. In blinded manner, responsible investigator or subinvestigator will investigate ocurring postoperative atrial fibrillation from ICU monitoring record.

Secondary

MeasureTime frame
30 day mortality, ischemic stroke, postoperative 48 hours over ventilation, acute kidney disease, rate of ischemic colitis, ICU stay, days of event postoperative atrial fibrillation, hospital stay, cost of ICU care, Hospital costs, VIS of intraoperative period and staying ICU period, total vasoactive use of intraoperative period and staying ICU period.

Contacts

Public ContactKochi Yamane

Nagoya University hospital

yama-anesth@med.nagoya-u.ac.jp+81-52-741-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026