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Effect of different blood pressure management strategies on postoperative delirium among elderly hypertensive patients undergoing non-cardiac surgery: a randomized controlled trial

Effect of different blood pressure management strategies on postoperative delirium among elderly hypertensive patients undergoing non-cardiac surgery: a randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057553
Enrollment
Unknown
Registered
2022-03-15
Start date
2022-07-19
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

postoperative delirium

Interventions

Experimental group:maintain SBP within ±10% of baseline
Control group:Patients will receive vasopressors in case of a drop in SBP below 90 mmHg or lower than 30% from the baseline

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients aged >=60 years; 2. ASA physical status II to III; 3. Patients with a history of hypertension; 4. Patients scheduled for major noncardiac surgery expected to last at least 2h under general anesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients with preexisting cognitive impairment; 2. Patients with severe neurologic conditions; 3. Patients with a major psychiatric condition such as bipolar disorder, major depression, schizophrenia, or dementia; 4. Patients with liver dysfunction (Child-Pugh grade C),renal failure,acute coronary syndrome,severe cardiac arrhythmias,acute or decompensated heart failure; 5. Patients with severely impaired visual, auditory or verbal communication; 6. Patients with a history of psychotropic substance abuse; 7. Patients with secondary hypertension; 8. Patients with severe uncontrolled hypertension(systolic blood pressure>=180mmHg or diastolic blood pressure>=110 mm Hg).

Design outcomes

Primary

MeasureTime frame
the incidence of postoperative delirium;

Secondary

MeasureTime frame
delirium duration and severity;postoperative duration of hospitalization;all-cause mortality;non-delirium complications;postoperative cognitive function;NRS pain scores both at rest and with movement;

Countries

China

Contacts

Public ContactSu Liu

The Affiliated Hospital of Xuzhou Medical University

150040009@qq.com+86 18118309692

Outcome results

None listed

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