Electronic alert for perioperative acute kidney injury

Electronic alert for perioperative acute kidney injury: pragmatic randomized controlled trial - E-alert AKI study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000040074

Enrollment

6000

Registered

2020-04-06

Start date

2020-06-01

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

acute kidney injury

Interventions

electronic AKI alert for detecting the increase of serum creatinine (0.3 mg/dL greater than or 50% greater than the lowest value) Control group: no alert (usual care)

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: adults aged 20 years or older who will undergo surgery under general anesthesia in Mie University Hospital

Exclusion criteria

Exclusion criteria: 1) no preoperative laboratory data including serum creatinine 2) preoperative creatinine 4.0 mg/dL or greater 3) patients with dialysis prior to surgery 4) emergency surgery 5) postponement of elective surgery 6) low risk surgery 7) can not obtain informed consent 8) invalid case

Design outcomes

Primary

Measure	Time frame
The incidence of acute kidney injury during postoperative 2 to 7 days.	—

Countries

Japan

Contacts

Public ContactHiroshi Yonekura

Mie University Hospital Department of Clinical Anesthesiology

hyonekura@clin.medic.mie-u.ac.jp059-231-5634

Outcome results

None listed

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