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The Effectiveness and Safety of Human Lumbar Puncture Assist Device (LPat)

NCT03710278 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 5

Last updated 2019-09-18

No results posted yet for this study

Summary

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.

Conditions

  • Meningitis
  • Encephalitis
  • Guillain-Barré
  • Subarachnoid Hemorrhage
  • Intracranial Neoplasm
  • Intracranial CNS Disorder

Interventions

DEVICE

LPat Device

Performing Lumbar Puncture utilizing LPat device

Sponsors & Collaborators

  • Edward Via Virginia College of Osteopathic Medicine

    collaborator OTHER

  • Spartanburg Regional Healthcare System

    lead OTHER

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-12-21
Primary Completion
2019-01-23
Completion
2019-01-23
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03710278 on ClinicalTrials.gov