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NCT05085509 Clinical Trial

Foreign Body Removal With the Assistance of Ultrasound Guidance and Methylene Blue Staining in Children

Ultrasound Clinical Trial

Official title:
Foreign Body Removal With the Assistance of Ultrasound Guidance and Methylene Blue Staining

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05085509
Other study ID # CQMU-20210016
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2016
Est. completion date December 31, 2020

Study information
Verified date October 2021
Source Children's Hospital of Chongqing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Soft-tissue foreign bodies (FB) are very commonly observed in pediatric emergency departments. Some are metallic and can be diagnosed easily via X-ray radiography, whereas others are radiolucent and are hence less easily diagnosed. Not all FB can be removed effectively, even via open surgery and C-arm guidance. This deficiency may potentially be addressed through the ultrasound (US) skills instrument, which is increasingly popular and is convenient for use in the operation room. In the current study, we evaluated the efficiency of FB removal with the assistance of US and methylene blue (MB) staining.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date December 31, 2020
Est. primary completion date May 1, 2016
Accepts healthy volunteers No
Gender All
Age group 1 Year to 18 Years
Eligibility Inclusion Criteria: - Diagnosed with soft-tissue foreign body - Must have complete clinical data Exclusion Criteria: - Had other injuries - Presented with more than 3 pieces foreign bodies

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• US guidance and MB staining
Ultrasound guidance and methylene blue staining

Locations
Country Name City State
China Children's Hospital of Chongqing Medical University Chongqing Chongqing

Sponsors (1)
Lead Sponsor Collaborator
Yuxi Su

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Surgery time Time from incision made to incision closure Surgery end time
Secondary Blood loss The blood loss of all the surgery time Surgery end time
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