Status:
UNKNOWN
The Effectiveness of a Pediatric Lumbar Puncture Restraint Device
Lead Sponsor:
University of Nebraska
Conditions:
Indication for Lumbar Puncture
Eligibility:
All Genders
1-90 years
Phase:
PHASE1
PHASE2
Brief Summary
This is a pilot study to evaluate a restraint device for lumbar punctures. Designed to help improve the restraint techniques for lumbar puncture, the restraint device will be compared to the current s...
Eligibility Criteria
Inclusion
- Age 1 to 90 days of life
- Indication for lumbar puncture procedure as determined by the treating physician
- Informed Consent from the subject's legal guardian indicating their acceptance of a lumbar puncture for the work-up of sepsis
- Informed consent to enrolled in said protocol
Exclusion
- No indication for lumbar puncture procedure as determined by treating physician
Key Trial Info
Start Date :
October 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 1 2014
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT00980070
Start Date
October 1 2009
End Date
June 1 2014
Last Update
June 21 2012
Active Locations (1)
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1
Childrens Hospital & Medical Center
Omaha, Nebraska, United States, 68114