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The Importance of Needle Size, Needle Design and Stylet Reinsertion to Prevent Post-lumbar Puncture Headache, a Randomized Controlled Trial
The objectives of this study are to investigate the effects of needle design, needle size and stylet reinsertion on the risk for headache after diagnostic LP (lumbar puncture, Post-LP headache). The following needles are used in the study: 1. Sprotte 25 Gauge (G) (0.5 mm) atraumatic needle with introducer 2. Sprotte 22 G (0.7 mm) atraumatic needle with introducer 3. Spinocan 25 G (0.5 mm) cutting needle
Age
16 - No limit years
Sex
ALL
Healthy Volunteers
No
Start Date
May 28, 2013
Primary Completion Date
June 24, 2018
Completion Date
October 11, 2018
Last Updated
May 23, 2019
1,000
ACTUAL participants
Sprotte 25G needle, stylet reinserted
DEVICE
Sprotte 25G needle, stylet not reinserted
DEVICE
Sprotte 22G needle, stylet reinserted
DEVICE
Sprotte 22G needle, stylet not reinserted
DEVICE
Spinocan 25G needle, stylet reinserted
DEVICE
Spinocan 25G needle, stylet not reinserted
DEVICE
Lead Sponsor
Jonatan Salzer
Collaborators
NCT06805591
NCT00373074
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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