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Impact of HPI-Guided Hemodynamic Management on the Duration and Severity of Postoperative Hypotension in Elderly Patients Undergoing Major Abdominal Surgery and Scheduled for AICU Admission: A Single-Center, Prospective, Open-Label, Randomized Controlled Clinical Trial

Impact of HPI-Guided Hemodynamic Management on the Duration and Severity of Postoperative Hypotension in Elderly Patients Undergoing Major Abdominal Surgery and Scheduled for AICU Admission: A Single-Center, Prospective, Open-Label, Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112603
Enrollment
Unknown
Registered
2025-11-17
Start date
2025-11-20
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Intraoperative hypotension (IOH)

Interventions

Control Group:Standard Care Group
Intervention Group:HPI-guided hemodynamic management

Sponsors

The Affiliated Drum Tower Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 65; 2.Scheduled for major abdominal surgery with planned AICU admission, and an anticipated procedure duration of >=2 hours and hospital stay of >=3 days; 3.To undergo invasive arterial blood pressure monitoring; 4.Willingness to participate in the study and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1.Refusal to participate in the study; 2.History of chronic alcoholism or substance dependence; 3.Severe cognitive impairment prior to surgery, as indicated by an MMSE score of 133 µmol/L, or ongoing dialysis; inability for self-care prior to surgery; 5.Cerebrovascular accident, myocardial infarction, or unstable angina within the past 3 months; 6.Severe hepatic dysfunction; 7.Neurological disorders, including dementia, Parkinson's disease, history of stroke with cognitive impairment, or long-term use of antipsychotic medications; 8.Surgery within the past 3 months; participation in another clinical trial within the past 30 days.

Design outcomes

Primary

MeasureTime frame
The difference in TWA between the two groups.;

Secondary

MeasureTime frame
Pain scores within 48 hours after surgery;The recovery rate of gastrointestinal function within 72 hours after surgery;Extubation time and AICU length of stay;The incidence of PONV within 48 hours after surgery;Myocardial Injury after Non-Cardiac Surgery (MINS);Postoperative Acute Kidney Injury (Postoperative AKI);Types of Intraoperative Hypotension;Postoperative Delirium (POD);The incidence and severity of IOH events;

Countries

China

Contacts

Public ContactXiaoping Gu

The Affiliated Drum Tower Hospital of Nanjing University Medical School

xiaopinggu@nju.edu.cn+86 25 83106666

Outcome results

None listed

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