NCT06546904

Brief Summary

Evaluate the effectiveness of AI powered anesthesia ultrasound in ultrasound-guided regional anesthesia (UGRA) training.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
5mo left

Started Sep 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress78%
Sep 2024Oct 2026

First Submitted

Initial submission to the registry

August 3, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 9, 2024

Completed
23 days until next milestone

Study Start

First participant enrolled

September 1, 2024

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 31, 2026

Last Updated

August 9, 2024

Status Verified

August 1, 2024

Enrollment Period

2 years

First QC Date

August 3, 2024

Last Update Submit

August 6, 2024

Conditions

Keywords

artificial intelligenceultrasound-guided regional anesthesia

Outcome Measures

Primary Outcomes (1)

  • Success rate of ultrasound-guided puncture

    Success rate of ultrasound-guided puncture at the first attempt

    1day

Secondary Outcomes (1)

  • Location time

    1day

Study Arms (2)

AI group

EXPERIMENTAL

Group AI used artificial intelligence to empower anesthesia ultrasound assisted simulated PNB operations in 5 areas

Device: Artificial intelligence empowers anesthesia with ultrasound assistance

Control group

NO INTERVENTION

Control group did not use AI assisted simulated PNB operations in 5 areas

Interventions

Artificial intelligence empowers anesthesia with ultrasound assistance

AI group

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Voluntary participants;
  • Sign the informed consent form.

You may not qualify if:

  • allergic to ultrasound coupling agents

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tongji hospital

Wuhan, Hubei, 430030, China

Location

Study Officials

  • mujun Chang, Dr.

    Tongji Hospital

    STUDY CHAIR

Central Study Contacts

aijun Xu, Dr.

CONTACT

aihua Du, Dr.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Professor

Study Record Dates

First Submitted

August 3, 2024

First Posted

August 9, 2024

Study Start

September 1, 2024

Primary Completion (Estimated)

August 31, 2026

Study Completion (Estimated)

October 31, 2026

Last Updated

August 9, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations