Tokyo, Aug. 29 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058904) titled 'Feasibility of Complete Real-Time Ultrasound-Guided Thoracic Epidural Puncture Using an Automatic LOR Detection Syringe: A Retrospective Observational Feasibility Study' on Aug. 29.
Study Type:
Observational
Primary Sponsor:
Institute - Omuta city hospital
Condition:
Condition - patients who underwent abdominal surgery with thoracic epidural anesthesia performed by real-time ultrasound-guided thoracic epidural puncture
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - This study focused on the technical feasibility of completely real-time ultrasound-guided thoracic epidural puncture using a syringe with an automatic resistance disappearance function, with particular emphasis on whether the moment of resistance disappearance (LOR) could be accurately visualized in real time under ultrasound guidance.
Basic objectives2 - Efficacy
Eligibility:
Age-lower limit - 18
years-old
<
Age-upper limit - Not applicable
Gender - Male and Female
Key inclusion criteria - We included all consecutive patients who underwent abdominal surgery and an attempt of real-time US-guided TEP during the study period.
Key exclusion criteria - The only exclusion criterion was puncture across the Th12/L1 level.
Target Size - 60
Recruitment Status:
Recruitment status - No longer recruiting
Date of protocol fixation - 2025 Year 08 Month 05 Day
Date of IRB - 2025 Year 08 Month 19 Day
Anticipated trial start date - 2025 Year 08 Month 19 Day
Last follow-up date - 2025 Year 09 Month 20 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067331
Disclaimer: Curated by HT Syndication.
