Skip to content

The impact of fluid resuscitation guided by the axillary vein collapse index under ultrasound guidance on the prognosis of elderly patients

The impact of fluid resuscitation guided by the axillary vein collapse index under ultrasound guidance on the prognosis of elderly patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106440
Enrollment
Unknown
Registered
2025-07-23
Start date
2025-02-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

None listed

Interventions

The fluid replacement group guided by the axillary vein collapse index:Fluid replacement guided by the axillary vein collapse index
The conventional fluid replacement group:Use conventional fluid replacement at a rate of 8 ml/kg/h

Sponsors

The First Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 65 or above, scheduled for laparoscopic cholecystectomy under general anesthesia; 2. ASA score ranging from 1 to 2; 3. Surgery duration of 2 to 6 hours; 4. No cognitive impairment before the operation, or if there is a mental disorder, but it has been well controlled for the past 6 months and the cognitive function is not impaired; 5. No damage to important organs such as heart, brain, or kidneys; 6. The patient and their family have agreed to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Patients with mental or neurological disorders; 2. Baseline mean arterial pressure (MAP) less than 65 mmHg; 3. Congestive heart failure with left ventricular ejection fraction less than 40%, acute or chronic renal failure, or other severe heart, lung, kidney or liver diseases; 4. Patients with coagulation disorders; 5. Patients who refuse to continue observation and withdraw from the experiment on their own; 6. Patients whose studies must be terminated due to significant hemodynamic fluctuations or severe anaphylactic shock during the perioperative period; 7. Patients lost to follow-up after discharge due to force majeure. 8. Anesthetic drug allergy sufferers.

Design outcomes

Primary

MeasureTime frame
The incidence of delirium during the recovery period;

Secondary

MeasureTime frame
Cognitive function score;VAS pain score;The first time to get out of bed for activities;The first time of anal exhaust;hospital stays;Postoperative adverse events;

Countries

China

Contacts

Public ContactYang Ling

Department of Anesthesiology, The First Hospital of Shanxi Medical University

YL1362367@163.com+86 136 2367 2056

Outcome results

None listed

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