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NCT06245239

Perfusion Index in Assessment of Postoperative Pain in Children.

Using Perfusion Index in Assessment of Postoperative Pain in Children Undergoing Hypospadias Repair Surgery: an Observational Follow up Study.
Assiut University·ClinicalTrials.gov·device·Device trialRecruiting
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Study focus
Disease/Condition
Postoperative Pain
Drug/Device/Intervention
perfusion index
Study type
Observational
Intervention type
device
Sponsor & location
Primary sponsor
Assiut University
Location
Assiut, Egypt
Timeline & enrollment
Phase
N/A
Start date
Feb 01, 2024
End date
Apr 01, 2024
Enrollment
65 participants
Primary outcome

Detection of the validity of Perfusion index in predicting Postoperative pain assessed by FLACC score

Summary

The aim of this study will be to examine the validity of perfusion index in predicting pain
 and evaluation of its severity in the postoperative period.

ICD-10 classifications
Acute painPostoperative intestinal obstructionPain, unspecifiedDuring surgical operationDuring surgical operation
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06245239
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT06245239 through Pure Global AI's free database. This phase not specified trial is sponsored by Assiut University and is currently Recruiting. The study focuses on Postoperative Pain. Target enrollment is 65 participants.

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