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UnknownNCT02590705

Anesthesia Lumbar Puncture In Children

Anesthesia Lumbar Puncture In Children (ALPIC)

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Beijing Children's Hospital · Academic / Other
Sex
All
Age
1 Month – 18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGLidocainesurface anesthesia with lidocaine

Timeline

Start date
2015-10-01
Primary completion
2016-09-01
Completion
2016-09-01
First posted
2015-10-29
Last updated
2015-10-29

Source: ClinicalTrials.gov record NCT02590705. Inclusion in this directory is not an endorsement.

Anesthesia Lumbar Puncture In Children (NCT02590705) · Clinical Trials Directory