Tokyo, June 20 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061979) titled 'A prospective observational study of the association between the level of supervisor oversight and the performance of peripheral intravenous cannulation by junior resident physicians' on June 19.
Study Type:
Observational
Primary Sponsor:
Institute - Fukuoka City Hospital
Condition:
Condition - Patients undergoing general anesthesia
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - The aim of this study is to evaluate the association between the timing of supervisor feedback (immediate versus delayed) and the success rate and procedure time of peripheral intravenous cannulation performed as part of routine clinical practice.
Basic objectives2 - Efficacy
Eligibility:
Age-lower limit - 18
years-old
<=
Age-upper limit - Not applicable
Gender - Male and Female
Key inclusion criteria - Patients undergoing peripheral intravenous cannulation before induction of general anesthesia
Key exclusion criteria - Emergency surgery
Shock
Severe dehydration
Severe edema
Patients in whom a supervising physician is unable to identify a suitable peripheral vein by visual inspection or palpation
Patients with a documented history of difficult peripheral intravenous cannulation
Target Size - 400
Recruitment Status:
Recruitment status - Open public recruiting
Date of protocol fixation - 2026 Year 06 Month 15 Day
Date of IRB - 2026 Year 06 Month 15 Day
Anticipated trial start date - 2026 Year 06 Month 16 Day
Last follow-up date - 2028 Year 03 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070915
Disclaimer: Curated by HT Syndication.
