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Clinical Trials/NCT03673475
NCT03673475CompletedNot Applicable

Internal Jugular Vein Distensibility and Pleth Variability Index for Evaluating Fluid Responsiveness

Tepecik Training and Research Hospital1 site in 1 country40 target enrollmentStarted: February 1, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
number of patients with significant change in VJI distensibility and pleth variebility index

Study Overview

Brief Summary

Assessment of intravascular volume status is crucial in order to predict the efficacy of volume status in major abdominal surgery. The aim of the study is to verify the feasibility and usefulness of the internal jugular vein distensibility index as an adjunct to the pleth variebility index(PVI) to predict fluid responsiveness in major abdominal surgery.

Detailed Description

Forty patients above age 18 and ASA status I-III who are undergoing major abdominal surgery will be enrolled in the study. patients with right heart failure, arrythmia, severe valve stenosis or regurgitation will be excluded. After induction of general anesthesia, when the patients are hemodynamically stabilised, PVI and jugular vein distensibility will be calculated and recorded. after volume load with 500 ml gel infusion(in 15 min), measurements will be repeated within 10 minutes and recorded. Patients will be allocated to 2 groups according to the change in mean arterial pressure(MAP) after volume expansion: Responders will be defined as an increase in MAP by >%10; while nonresponders will be defined as an increase in MAP <%10 or decrease in MAP.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • American Society of Anesthesiologists(ASA) physical status I-III patients
  • patients undergoing major abdominal surgery

Exclusion Criteria

  • arrythmia
  • severe right ventricle failure

Outcomes

Primary Outcomes

number of patients with significant change in VJI distensibility and pleth variebility index

Time Frame: during surgery at day 0

volume responders with significant change in jugular vein distensibility and pleth variebility index

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Tepecik Training and Research Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

MELTEM CAKMAK

Anesthesiologist

Tepecik Training and Research Hospital

Study Sites (1)

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