NCT06290752

Brief Summary

mastering ultrasound-guided sacral canal block entails traversing a multifaceted learning curve characterized by anatomical intricacies, technical challenges, and patient variability. Through systematic education, deliberate practice, and clinical experience, clinicians can ascend this learning curve and harness the full potential of this innovative technique in pain management. As the landscape of regional anesthesia continues to evolve, a commitment to ongoing learning and proficiency attainment is paramount for delivering safe, effective, and patient-centered care.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
6

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
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

First Submitted

Initial submission to the registry

February 26, 2024

Completed
4 days until next milestone

Study Start

First participant enrolled

March 1, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 4, 2024

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
Last Updated

March 12, 2024

Status Verified

March 1, 2024

Enrollment Period

9 months

First QC Date

February 26, 2024

Last Update Submit

March 7, 2024

Conditions

Anesthesia

Outcome Measures

Primary Outcomes (1)

  • operation time

    Operating time of students from starting scan to nerve block completion

    15 minutes

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Residential trainee

You may qualify if:

  • Residential training students in the first -third grade

You may not qualify if:

  • No-resident trainees

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dongmei Ma

Yiwu, Zhejiang, 322000, China

RECRUITING

Study Officials

  • Dongmei Ma

    浙江大学医学院附属第四医院

    STUDY CHAIR

Central Study Contacts

Zhu Xinqiang, DR

CONTACT

+865798993505265602423@qq.com

Dongmei Ma

CONTACT

+86152673580778019111@zju.edu.cn

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 26, 2024

First Posted

March 4, 2024

Study Start

March 1, 2024

Primary Completion

November 30, 2024

Study Completion

December 31, 2024

Last Updated

March 12, 2024

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will not share

Locations

CN(1)