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Clinical study for evaluating the accuracy of preoperative blood volume and the rationality of fluid replacement in elderly patients by ultrasonic measurement of the inferior vena cava collapse index

Clinical study for evaluating the accuracy of preoperative blood volume and the rationality of fluid replacement in elderly patients by ultrasonic measurement of the inferior vena cava collapse index

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026267
Enrollment
Unknown
Registered
2019-09-28
Start date
2019-10-01
Completion date
Unknown
Last updated
2019-09-30

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

Conditions

hypotension

Interventions

Control group:Rehydrate according to '421 rehydration method'
Experimental group:For patient with insufficiency of blood volume, 250ml hydroxyethyl starch was given and transfused in 10 minutes. Measure ICV-CI again until the rehydration is normal, and then rehy

Sponsors

The First Affiliated Hospital of Shihezi University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 89 Years

Inclusion criteria

Inclusion criteria: Patients undergoing elective anesthesia surgery; aged 65-89 years old; American Academy of anesthesiologists (ASA) grade I ~ II; BMI 18 <=25 kg/m2; patients and their families knew and signed informed consent; patients were conscious and breathing autonomously; patients volunteered to be measured; patients were not covered with gauze or bandages.

Exclusion criteria

Exclusion criteria: Emergency surgical patients;Peripheral vascular disease, severe cardiovascular disease, unstable angina pectoris or ejection fraction less than 40%; Patients with respiratory distress, increased abdominal pressure, expected airway or mental dysfunction; Patients with autonomic nervous system disease; Patients with implantable pacemakers or rhythm converters; Lower vena vena disease, hypertension patients taking angiotensin conversion enzyme inhibitors or angiotensin receptor antagonists; Preanesthetic basic SBP<90mmHg;Sudden change of vital signs before operation, life-threatening patients; Waist anesthesia taboos.

Design outcomes

Primary

MeasureTime frame
Diameter and collapse rate of inferior vena cava.;hypotension;Norepinephrine dosage;

Secondary

MeasureTime frame
cardiac output;

Countries

China

Contacts

Public ContactZhang Yu

The First Affiliated Hospital of Shihezi University Medical College

2455645947@qq.com+86 18334532797

Outcome results

None listed

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