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Anesthesia Lumbar Puncture In Children — ALPIC  

Anesthesia Clinical Trial

Official title:
Anesthesia Lumbar Puncture In Children (ALPIC)

Clinical Trial Summary

The study is carried out in a prospectively randomly controlled way. In the context of acknowledgement and understanding from parents, by comparing with traditional process(no anesthesia), lidocaine surface anesthesia is randomly selected. All children will be evaluated by the FLACC (The face, legs, activity, cry, consolability behavioral tool) scale to quantitatively assess degree of pain during lumbar puncture. Time and success rate of the lumber puncture will be recorded and analyzed. A questionnaire about bad memory during lumbar puncture for all parents and children will be investigated in order to establish an optimized lumbar puncture management process.

Clinical Trial Description

The purpose of this study is to establish an optimized lumbar puncture management process on the basis of fully understanding of parents and children. An improved process consisting of painless lumbar puncture (LP) and comfortable LP will be established upon completion of this study. ;

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02590705
Study type Interventional
Source Beijing Children's Hospital
Contact Bing Hu, postgraduate
Email hubing6028@163.com
Status Not yet recruiting
Phase N/A
Start date October 2015
Completion date September 2016
View Details
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