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Internal Jugular Venous Distensibility Index and Innominate Venous Flow Patterns As Predictors of Fluid Responsiveness

U

University of Indonesia (UI)

Status

Completed

Conditions

Hemodynamic Monitoring
Fluid Responsiveness

Treatments

Device: Ultrasonography of Internal Jugular Vein
Device: Doppler Echocardiograhy

Study type

Observational

Funder types

Other

Identifiers

NCT05930600
IndonesiaUAnes044

Details and patient eligibility

About

The measurement of internal jugular vein distensibility index corresponds to the measurement of stroke volume using trans-thoracic Doppler echocardiography in assessing the response to fluid administration in elective surgical patients.

Enrollment

79 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Utilizing intraoperative mechanical ventilation with a tidal volume of 8 ml/kg (PBW).
  2. ASA physical status 1-3.
  3. Mongoloid ethnicity.
  4. Willing to participate in the research and sign the informed consent.

Exclusion criteria

  1. Patients with symptoms and signs of fluid overload, such as pulmonary edema, pleural effusion, ascites, and peripheral edema.
  2. Patients with chronic or acute kidney dysfunction, renal replacement therapy history, and/or oliguria (urine output <0.5 ml/kg/hour).
  3. Patients with cardiovascular diseases, including heart failure, cardiac arrhythmias, moderate-to-severe valvular abnormalities, a history of angina/myocardial infarction, pulmonary hypertension, and peripheral artery disease.
  4. Patients with anatomical abnormalities in the neck and chest region that make it impractical to perform jugular vein ultrasound and transthoracic echocardiography.
  5. Jugular vein thrombosis.
  6. Superior vena cava syndrome.
  7. Placement of jugular vein catheter.
  8. Body mass index (BMI) greater than 30.0 kg/m2.
  9. Patients with contraindications to the use of muscle relaxants.
  10. Patients with lung hyperinflation and pleural effusion.

Drop out criteria:

  1. Patients who wish to withdraw from the study.
  2. Post-anesthesia induction complications and emergencies.
  3. Transthoracic echocardiography provides a less representative image due to difficult acoustic window.

Trial contacts and locations

1

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Central trial contact

Dita Aditianingsih

Data sourced from clinicaltrials.gov

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