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Epidural Waveforms: Pressure Transducer vs CompuFlo

NCT04240197 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2022-03-23

No results posted yet for this study

Summary

The purpose of this single arm, open label study will be to compare and evaluate the sensitivity and specificity of CompuFlo to detect epidural pulse waveforms (EPW) to assess the correct placement of the catheter in the epidural space when compared to the standard pressure transducer.

Conditions

  • Anesthesia

Interventions

DEVICE

CompuFlo

The occurrence of epidural pulse waves with CompuFlo and with standard pressure trnsducer

Sponsors & Collaborators

  • European e-Learning School in Obstetric Anesthesia

    lead OTHER

Principal Investigators

  • Giorgio Capogna, MD · European e-Learning School in Obstetric Anesthesia

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-01
Primary Completion
2021-04-30
Completion
2021-04-30
FDA Device
Yes

Countries

  • Italy

Study Locations

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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 NCT04240197 on ClinicalTrials.gov