Tokyo, March 25 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061035) titled 'Pilot study of the additional effect of cadaver training in video laryngoscope intubation education for first-year postgraduate residents' on March 25.

Study Type: Interventional

Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Open -no one is blinded Control - Active

Primary Sponsor: Institute - Niigata University Medical and Dental Hospital

Condition: Condition - Healthy volunteers (first-year postgraduate residents) Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - To exploratorily examine whether adding pretreated formalin-fixed cadaver training to standard mannequin-based video laryngoscope intubation training improves the magnitude of patient-imagined self-efficacy for video laryngoscope intubation among first-year postgraduate residents. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - Control group Standard mannequin-based video laryngoscope intubation training using the McGRATH video laryngoscope. Each participant will perform 2 intubation attempts on a mannequin. Interventions/Control_2 - Intervention group Standard mannequin-based video laryngoscope intubation training using the McGRATH video laryngoscope, plus additional pretreated formalin-fixed cadaver training. Each participant will perform 2 intubation attempts on a mannequin and 2 cadaver intubation attempts on 2 different pretreated formalin-fixed cadavers, 1 attempt per cadaver, according to a pre-specified rotation schedule.

Eligibility: Age-lower limit - Not applicable Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - First-year postgraduate residents (PGY1) undergoing clinical training at the study institution during the study year Participants with no prior clinical experience in tracheal intubation, or no prior clinical experience in video laryngoscope intubation Written informed consent obtained based on free will after study explanation Key exclusion criteria - Participants unable to attend the training session because of poor physical condition or other reasons Pregnant participants Participants judged inappropriate by the principal investigator for safety or operational reasons Target Size - 12

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2026 Year 03 Month 01 Day Anticipated trial start date - 2026 Year 04 Month 01 Day Last follow-up date - 2026 Year 04 Month 01 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000069845

Disclaimer: Curated by HT Syndication.