Clinical Trials Directory

Trials / Unknown

UnknownNCT02590718

Management Following Lumbar Puncture In Children

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 (lying without the pillow and fasting water and food for four hours following lumbar puncture), an optimized postoperative management (lying without the pillow for half an hour following lumbar puncture) is randomly selected. All children will be evaluated by the FLACC (The face, legs, activity, cry, consolability behavioral tool) scale to assess the degree of pain after lumbar puncture. Any postoperative condition will be recorded and analyzed. A questionaire 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 comfortable LP will be established upon completion of this study.

Conditions

Interventions

TypeNameDescription
PROCEDUREoptimized postoperative managementlying without the pillow for half an hour after lumbar puncture

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 NCT02590718. Inclusion in this directory is not an endorsement.