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NCT03094754 Clinical Trial

Excision Size and Location on the Postoperative Pain After Nevi Excision in Children

Anesthesia, Endotracheal Clinical Trial

Official title:
Effect of Excised Surface Area/Body Surface Area Ratio and Location of Excision on the Postoperative Pain After Nevi Excision in Children: Observational Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03094754
Other study ID # AJIRB-MED-OBS-16-533
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 13, 2017
Est. completion date January 25, 2018

Study information
Verified date December 2018
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary purpose of this study is to investigate the effects of excised surface area/body surface area ratio and location of excision on the postoperative pain after nevi excision in children.

The primary purpose of this study is to investigate the effects of excised surface area/body surface area ratio and location of excision on the emergence excitation after nevi excision in children.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date January 25, 2018
Est. primary completion date January 25, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Year to 7 Years
Eligibility Inclusion Criteria:

- children undergoing nevi excision on general anesthesia

Exclusion Criteria:

- development disorder

- neurological disorder

- psychological disorder

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• nevi excision
After general anesthesia, nevi excision in children is performed.

Locations
Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Ajou University School of Medicine Suwon Seoum

Sponsors (1)
Lead Sponsor Collaborator
Ajou University School of Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary postoperative pain score postoperative pain score after nevi excision up to 3 hours
Secondary emergence agitation score emergence agitation score after nevi excision up to 3 hours
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