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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05721157
Other study ID # NDMC2023001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2023
Est. completion date June 30, 2023

Study information

Verified date July 2023
Source National Defense Medical Center, Taiwan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Artificial Intelligence-assisted Diagnosis and Prognostication in Osteoporosis Using Chest X-ray


Recruitment information / eligibility

Status Completed
Enrollment 4912
Est. completion date June 30, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: - Patients recieved at least 1 chest X-ray examination in 2022 - More than 66% chest X-ray identified as high risk of osteoporosis by AI-CXR Exclusion Criteria: - Patients with history of at least 1 dual energy x-ray absorptiometry (DXA) - Patients with history of osteoporosis or osteoportic fracture - Patients recieved prescription anti-osteoporotic treatment (excluding vitamin D or calcium) - Patients died before 01 Jan 2023

Study Design


Related Conditions & MeSH terms


Intervention

Other:
AI-enabled Chest X-ray-based Screening Tool
Primary care clinicians in the intervention group had access to the report, which displayed whether the AI-Chest X-ray result was positive or negative.The system will send a message to corresponding physicians if positive finding.

Locations

Country Name City State
Taiwan Tri-service general hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Defense Medical Center, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary newly diagnosed with osteoporosis After performing an chest X-ray, the osteoporosis was followed. Within 180 days
Secondary initiation of DXA examination After performing an chest X-ray, the osteoporosis was followed. Within 180 days
Secondary initiation of anti-osteoporotic treatment After performing an chest X-ray, the osteoporosis was followed. Within 180 days
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