Performance of Artificial Intelligence Tools and Ultrasonographers With Different Skills (PAITUWDS)

April 9, 2023 updated by: Hongkui Yu, MD

Comparison of Artificial Intelligence and Ultrasonographers With Different Skills in Diagnosing Intussusception in Children and Identifying Indications for Surgery

Artificial intelligence versus different skilled sonographers.

Study Overview

Detailed Description

Comparison of artificial intelligence and ultrasonographers with different skills in diagnosing intussusception in children and identifying indications for surgery.

Study Type

Observational

Enrollment (Anticipated)

250

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Guangdong
      • Guangzhou, Guangdong, China, 510623
        • Recruiting
        • Hongkui Yu, MD
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Children aged 3-36 months with suspected ileocolic intussusception

Description

Inclusion Criteria:

  • Children aged 3-36 months with suspected ileocolic intussusception

Exclusion Criteria:

  • Children younger than 3 months or older than 36 months with suspected ileocolic intussusception

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients aged 3-36 months with suspected ileocolic intussusception
Non-invasive diagnosis of ileocolic intussusception by ultrasound with indication for surgery

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ultrasound diagnosis of ileocolic intussusception
Time Frame: April 9, 2023 to May 10, 2023
Ultrasound diagnosis of ileocolic intussusception
April 9, 2023 to May 10, 2023

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Surgical indication of ileocolic intussusception identified by ultrasound
Time Frame: April 9, 2023 to May 10, 2023
Surgical indication of ileocolic intussusception identified by ultrasound
April 9, 2023 to May 10, 2023

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hongkui Yu,, Guangzhou Women and Children's Medical Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 9, 2023

Primary Completion (Anticipated)

May 10, 2023

Study Completion (Anticipated)

May 10, 2023

Study Registration Dates

First Submitted

April 9, 2023

First Submitted That Met QC Criteria

April 9, 2023

First Posted (Actual)

April 21, 2023

Study Record Updates

Last Update Posted (Actual)

April 21, 2023

Last Update Submitted That Met QC Criteria

April 9, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • GuangzhouWCMC20230409

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

For non-commercial use in research, you can contact Prof. Hongkui Yu to get the data at hongkuiyu@126.com.

IPD Sharing Time Frame

After May 20, 2023

IPD Sharing Access Criteria

For non-commercial use in research, you can contact Prof. Hongkui Yu to get the data at hongkuiyu@126.com.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ANALYTIC_CODE

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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