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A randomized, single blind, controlled, single center clinical trial was designed to compare the effects of IVC-CI guided fluid infusion and conventional fluid infusion on blood pressure in elderly patients after induction of general anesthesia

Effects of IVC-CI guided fluid infusion and routine fluid infusion on blood pressure in elderly patients after induction of general anesthesia

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069834
Enrollment
Unknown
Registered
2023-03-27
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Hypotension after general anesthesia

Interventions

Rapid rehydration group:Before operation, rapid fluid infusion should be carried out for patients with collapse index of inferior vena cava = 43%
Control group:Conventional crystal liquid infusion

Sponsors

Zhujiang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 60 and above; 2. ASA Class I-III; 3. Non cardiac surgery is planned under general anesthesia; 4. The collapse index of inferior vena cava = 43% 30 minutes before operation.

Exclusion criteria

Exclusion criteria: 1. Patients with heart, brain, lung, liver, kidney and other important organ dysfunction 2. Severe peripheral vascular disease, portal hypertension, hypertension taking angiotensin converting enzyme inhibitors or angiotensin receptor blockers. 3. Patients with difficult airway 4. Patients who cannot tolerate rehydration therapy

Design outcomes

Primary

MeasureTime frame
Triple A;Incidence of hypotension;

Secondary

MeasureTime frame
Vital signs;Adverse reactions;

Countries

China

Contacts

Public ContactYihong Lei

Zhujiang Hospital of Southern Medical University

Lhy2012@smu.edu.cn13143506862

Outcome results

None listed

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