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NCT06667401 · ClinicalTrials.gov registry record
Exploring the Efficacy of Assistive Artificial Intelligence for Ultrasound Guided Regional Anesthesia in Residency Training
A clinical trial, sponsored by Medical College of Wisconsin.
- Completed
- Registry status
- 20
- Enrollment target
NCT06667401: Completed study, sponsored by Medical College of Wisconsin.
NCT06667401 is a clinical trial that has completed, run by Medical College of Wisconsin. The registered enrollment target is 20 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06667401 has completed, sponsored by Medical College of Wisconsin.
- COMPLETED
- Registry status
- 20 participants
- Enrollment target
Study Summary
The purpose of this study is to investigate the efficacy of a novel artificial intelligence (AI) device designed to assist in Ultrasound guided regional anesthesia (ScanNav Anatomy Peripheral Nerve Block; ScanNav), in the teaching and training of anesthesiology residents in the subspecialty of regional anesthesia.
Primary Outcome
Improved teaching and training of anesthesiology residents in the subspecialty of regional anesthesia will be accessed via a questionnaire filled out by participants after use of the device. The questionnaire will access, the type of regional blocks, feasibility of block and ease of teaching with the artificial intelligence Ultrasound.
Interventions
- DEVICE The ScanNav, a novel artificial intelligence device designed to assist in Ultrasound guided regional anesthesia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2025-03-10 |
| Est. Completion | 2026-01-01 |
What the finished NCT06667401 record still lists
NCT06667401 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which The ScanNav, a novel artificial intelligence device designed to assist in Ultrasound guided regional anesthesia is the first listed.
NCT06667401 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06667401 about?
NCT06667401 is a clinical study titled "Exploring the Efficacy of Assistive Artificial Intelligence for Ultrasound Guided Regional Anesthesia in Residency Training". The purpose of this study is to investigate the efficacy of a novel artificial intelligence (AI) device designed to assist in Ultrasound guided regional anesthesia (ScanNav Anatomy Peripheral Nerve Block; ScanNav), in the teaching and training of anesthesiology residents in the subspecialty of regio...
What is the current status of trial NCT06667401?
This trial is currently completed. The enrollment target is 20 participants. The study started on 2025-03-10. Estimated completion is 2026-01-01.
What interventions are being tested in trial NCT06667401?
The interventions under investigation include: The ScanNav, a novel artificial intelligence device designed to assist in Ultrasound guided regional anesthesia (DEVICE).
Who is sponsoring clinical trial NCT06667401?
This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.
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