AR for Pediatric Central Venous Catheterization

  • STATUS
    Recruiting
  • participants needed
    120
  • sponsor
    Seoul National University Hospital
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Updated on 16 February 2024
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Summary

This study is intended to investigate usefulness of smart-glasses for ultrasound-guided central venous catheterization in pediatric patients, by comparing success rate and elapsed time. The hypothesis is that smart-glasses would increase success rate in first trial.

Description

After obtaining informed consent from patients' legal guardian, children aged 6 or less undergoing surgery with need for central venous catheterization will be enrolled to the study.

Patients will be divided into either study group or control group. After anesthetic induction, central venous catheterization will be performed under ultrasound guidance. For patients in study group, the practitioner will be equipped with smart-glasses, while conventional ultrasound-guided catheterization will be performed for patients in control group.

Success rate of first trial, overall success rate, elapsed time during catheterization, complication regarding catheterization will be recorded and compared.

Details
Condition Anesthesia, Anesthesia
Age 6years or below
Treatment Smart glass
Clinical Study IdentifierNCT04378166
SponsorSeoul National University Hospital
Last Modified on16 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

Patients who are planned to undergo surgery under general anesthesia
Patients in need for central venous catheterization during anesthesia

Exclusion Criteria

Patients who have any of infection, hematoma, skin lesion, recent attempt of puncture at right internal jugular vein
Patients with unstable vital sign prior to anesthetic induction
Patients who are not eligible for catheterization at right internal jugular vein
Refusal of legal guardian of patient
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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