Hemostasis Using Radiofrequency Ablation for Track Bleeding

  • STATUS
    Recruiting
  • End date
    Dec 31, 2024
  • participants needed
    10
  • sponsor
    Kyoung Doo Song
Updated on 30 August 2021
haemostasis

Summary

This study aims to evaluate the usefulness of hemostasis using radiofrequency ablation for track bleeding that has occurred after percutaneous biopsy of the liver.

Description

Purpose: To evaluate the usefulness of hemostasis using radiofrequency ablation for track bleeding after percutaneous liver biopsy.

Method
  • Enroll patients who continue to bleed despite conservative treatment for track bleeding that has occurred after liver biopsy.
  • Radiofreqeuncy ablation: Under monitoring vital signs and controlling pain with intravenous agents, the electrode is inserted into the bleeding focus. The bleeding focus is ablated.
  • Hemostasis is evaluated by ultrasound (right after radiofrequency ablation), CT scan (after the radiofrequency ablation), and ultrasound (the day after radiofrequency ablation)
  • If hemostasis fails using radiofrequency ablation, transarterial hepatic embolization is performed immediately.

Details
Condition Hemorrhage
Treatment Radiofrequency ablation
Clinical Study IdentifierNCT05017350
SponsorKyoung Doo Song
Last Modified on30 August 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Ultrasound guided percutaneous liver biopsy at Samsung Medical Center
Track bleeding after biopsy
Persistent track bleeding even after conservative management
Consent to this study

Exclusion Criteria

Not consent to this study
<20 years old or >=80 years old
Contraindication to radiofrequency ablation
Radiofrequency ablation for track bleeding is not technically possible
Unstable vital signs
Clear my responses

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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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