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Prediction of intraoperative hypotension in liver resection using the Hypotension Prediction Index

Examination of the effectiveness of the Hypotension Prediction Index in preventing hypotension during surgery in patients undergoing liver resection -A randomized, open-label, standard monitoring-controlled, parallel-group comparative study-

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1032240727
Enrollment
68
Registered
2025-03-12
Start date
2025-06-26
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

Resectable liver cancer

Interventions

Test equipment group: Circulation monitoring during surgery will be performed using an HPI system consisting of a dedicated sensor (Acumen IQ sensor) and monitor (HemoSphere). Standard equipment group

Sponsors

Ishikawa Seiji
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients aged 18 years or older and 80 years or younger at the time of obtaining consent 2) Patients diagnosed with liver cancer at the time of obtaining consent 3) Patients scheduled to undergo liver resection under general anesthesia 4) Inpatients 5) Patients who have the capacity to consent and can provide written consent of their own free will 6) Patients with ASA PS 1 to 3 7) Patients who the principal investigator (subinvestigator) judges to be able to appropriately evaluate the efficacy and safety of this study after considering the inclusion and exclusion criteria

Exclusion criteria

Exclusion criteria: 1) Patients who cannot undergo epidural anesthesia 2) Patients for whom invasive blood pressure monitoring is contraindicated 3) Patients with severe cardiac disease (left ventricular ejection fraction less than 40%) or pulmonary disease (forced expiratory volume in 1 second less than 40%) 4) Patients undergoing renal replacement therapy, including hemodialysis 5) Patients with atrial fibrillation 6) Patients with moderate or severe aortic or mitral valve stenosis or regurgitation 7) Pregnant women or women who may be pregnant 8) Breastfeeding women 9) Other patients who the principal investigator (subinvestigator) deems inappropriate to be study subjects

Design outcomes

Primary

MeasureTime frame
Time-weighted average of hypotension (mean blood pressure < 65mmHg) during surgery

Secondary

MeasureTime frame
1) Number of hypotension events (mean blood pressure < 65mmHg) during surgery (hypotension lasting for 1 minute or more is counted as 1 event) 2) Total time of hypotension (mean blood pressure < 65mmHg) during surgery (intraoperative hypotension duration) (events lasting less than 1 minute are not taken into account) 3) Average time per event of hypotension (mean blood pressure < 65mmHg) during surgery (mean intraoperative hypotension duration) 4) Percentage of time of hypotension (mean blood pressure < 65mmHg) to total monitoring time (from start of circulatory monitoring to end of anesthesia) 5) Area under the curve below the hypotension threshold (65mmHg) when the vertical axis is blood pressure and the horizontal axis is monitoring time 6) Incidence rate of acute kidney injury (KDIGO criteria) occurring within 72 hours after surgery

Contacts

Public ContactSeiji Ishikawa

Juntendo University, Juntendo Hospital

se-ishikawa@juntendo.ac.jp+81-3-3813-3111

Outcome results

None listed

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