Actively Recruiting

Phase Not Applicable
Age: 60Years - 80Years
All Genders
NCT06641505

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

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

80

Participants Needed

1

Research Sites

43 weeks

Total Duration

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AI-Summary

What this Trial Is About

Compare the incidence of hypotension during the propofol-induced period between the internal jugular vein variability-guided fluid infusion group and the conventional fluid infusion group through a fluid infusion experiment before anesthesia induction, so as to evaluate the feasibility of using the internal jugular vein variability under deep inspiration to guide preoperative fluid infusion.

CONDITIONS

Official 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
  • 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) 30 kg/m2 or higher
  • Short neck
  • 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 surgery on the neck
  • Unable to lie flat for necessary measurements
  • Mechanical ventilation or inability to take deep breaths
  • History of gastrointestinal surgery
  • Allergy to propofol
  • Restricted fluid intake

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

CONTACT

X

Xuelian Wei

CONTACT

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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