About this trial
A research trial which compares standard of care against employing a novel device for immobilization of babies undergoing upright LP, the present working name for the device is LP Comfort Seat (LPCS).
The research question is:
P: In late-preterm to term babies who are 0-28 days and undergoing LP for R/O Sepsis I: Is the LPCS more effective C: Than human/RN assisted upright positioning O: In generating a higher rate of first attempt LP success
Primary outcome measure is first attempt LP success (any evidence of CSF which is diagnostically useful by content and volume)
Secondary outcome measures could include
1. A qualitatively unadulterated tap (no blood) although as you know this is hard to control even with perfect positioning and technique and single pass 2. A difference in FLACC score as measure of overall pain/comfort between test and control
Eligibility criteria
Qualifiers
Late preterm (34 + weeks) Gestational Age to Term (42+ weeks GA)
Weight of 2.5 - 5 kg
Disqualifiers
Any contraindication to having a lumbar punture procedure
Trial design
Treatments tested in this trial
- A novel device for immobilization of babies undergoing upright LP, the present working name (non-proprietary) for the device is LP Comfort Seat (LPCS)
- Standard of Care (SOC)
Treatment groups
Locations
Sponsors and collaborators
Joel Cox
Lead sponsor
Nova Scotia Health Authority
Sponsor institution
Nova Scotia Health Authority
Collaborator