Actively Recruiting

Phase Not Applicable
Age: 60Years - 80Years
All Genders
ID06641505

Feasibility of Deep Inspiratory Internal Jugular Vein Variability in Guiding Preoperative Fluid Replacement: A Prospective, Randomized Controlled Study

Led by Affiliated Hospital of Jiaxing University · Updated on 2024-11-15

80

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating whether using the variability of the internal jugular vein during deep inspiration can guide fluid infusion before anesthesia to reduce the risk of low blood pressure caused by propofol. This prospective, randomized controlled study compares this method against conventional fluid infusion techniques in adults aged 60 to 80 undergoing surgery. The study aims to assess the feasibility of using ultrasound measurements to direct preoperative fluid replacement safely. Participants receive fluid infusion guided by the internal jugular vein variability based on the 421 fluid replacement principle or conventional fluid infusion at a rate of 0.2 ml/kg/min for 15 minutes before anesthesia induction. Propofol is infused with a target-controlled concentration of 4 bcg/ml, and blood pressure changes within three minutes after induction are monitored. The study includes two groups: one with variability-guided fluid replacement and one with conventional fluid replacement. During the study, ultrasound is used to record breathing cycles to calculate vein variability, and arterial blood pressure is closely observed after propofol administration. Researchers monitor the incidence of a 20% drop in blood pressure as the primary outcome over one year. The trial requires surgery with radial artery puncture and careful monitoring of anesthesia induction effects. Participation lasts through the preoperative fluid infusion, anesthesia induction, and immediate monitoring periods.

CONDITIONS

Brief Title

Feasibility of Deep Inspiratory Internal Jugular Vein Variability in Guiding Preoperative Fluid Replacement

Who Can Participate

Age: 60Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 60 years and up to 80 years
  • American Society of Anesthesiology (ASA) status I-II
  • Scheduled for surgery with radial artery puncture
  • Planned propofol anesthesia induction
Not Eligible

You will not qualify if you...

  • Body mass index (BMI) of 30 kg/m2 or higher
  • Short neck anatomy
  • History of low blood pressure (systolic <90 mmHg or mean arterial pressure <65 mmHg)
  • Poorly controlled hypertension
  • Cardiac insufficiency with ejection fraction less than 50%
  • Upper limb deep vein thrombosis
  • History of radiotherapy or neck surgery
  • Unable to lie supine for necessary measurements
  • Mechanical ventilation or inability to take deep breaths
  • History of gastrointestinal surgery
  • Allergy to propofol
  • Restricted fluid intake

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 15 minutes

Participants receive preoperative fluid rehydration according to assigned fluid replacement principles before anesthesia induction.

1 visit (in-person)

Follow-up

Duration - 3 minutes

Participants are monitored for changes in blood pressure within 3 minutes after propofol anesthesia induction.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Affiliated Hospital of University

Jiaxing, Zhejiang, China

Actively Recruiting

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Research Team

Q

Qinghe Zhou

X

Xuelian Wei

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Effects of liquid resuscitation guided by internal jugular vein variability during deep inhalation on preventing propofol-induced hypotension in elderly patients.

Xue-Lian Wei, Ya-Zhi Xi, Lei Xie...

https://pubmed.ncbi.nlm.nih.gov/40676549