Optimization Lumbar Puncture In Children

• Status: Withdrawn
• Trial end date: 2016-03-01
• Target enrollment: 0
• Participant gender: All

Summary

The study is carried out in a prospective randomized controlled way. In the context of informed understanding from parents, compared with traditional process(no anesthesia; lying without the pillow and fasting water and food for four hours after lumbar puncture), randomly select lidocaine surface anesthesia and postoperative management (lying without the pillow for half an hour after lumbar puncture) . All children will be evaluated by the FLACC(The face,legs,activity,cry,consolability behavioral tool) scale to assess the degree of pain during and after lumbar puncture. Lumber puncture time, success rate and any postoperative condition will be recorded and analyzed.A questionaire about the operation for all parents and children will be investigated in order to establish an optimized lumbar puncture management process.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Beijing Children's Hospital
• Treatments: Lidocaine

Criteria

Inclusion Criteria:

• children with indications of lumbar puncture;

• voluntarily signed the informed consent

Exclusion Criteria:

• topical anesthetic skin allergies;

• skin infection in lumbar puncture site;

• severe intracranial hypertension;

• unstable vital signs;

• coagulopathy;

• intracranial hemorrhage and occupying;

• low back pain;

• headache and low back pain before lumbar puncture;

• past headache after lumbar puncture;

• mental retardation, neuropsychiatric symptoms;

• children could not immediately act after the lumbar puncture(such as disturbance of consciousness or suffering from underlying diseases or drainage);

• the case with repeated puncture in one operation