Subarachnoid Hemorrhage Clinical Trial
— LPatOfficial title:
The Effectiveness and Safety of Human Lumbar Puncture Assist Device (LPat)
Verified date | September 2019 |
Source | Spartanburg Regional Healthcare System |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to proof and investigate the effectiveness and safety of the invented device named "Human Lumbar Puncture Assist Device (LPat)" as an assist tool to be utilized to improve the success rate of performing lumbar puncture (LP), avoid side effects from multiple punctures, avoid excess radiation if the LP need to be done under fluoroscopy, and need to obtain none traumatic tap for better CSF analysis.
Status | Completed |
Enrollment | 5 |
Est. completion date | January 23, 2019 |
Est. primary completion date | January 23, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 12 Years and older |
Eligibility |
Inclusion Criteria: Patients age 12 years and older who need lumbar puncture (LP) for diagnostic purposes or patients already underwent LP but failed to obtain Cerebrospinal Fluids i.e. "Unsuccessful Tap" Exclusion Criteria: Patients younger than 12 years of age |
Country | Name | City | State |
---|---|---|---|
United States | Spartanburg Reginal Heathcare System | Spartanburg | South Carolina |
Lead Sponsor | Collaborator |
---|---|
Spartanburg Regional Healthcare System | Edward Via Virginia College of Osteopathic Medicine |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Successful Lumbar Puncture | Obtain CSF | Immediate |
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