MedTrace Logo

Epidural Computer Controlled System for the Epidural Space Verification

NCT03165708 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2017-05-24

No results posted yet for this study

Summary

The purpose of this study will be to evaluate the inter-rater agreement, or concordance, between an expert anaesthesiologist and the CompuFlo® Epidural Computer Controlled System for the epidural space verification.

Primary study endpoint will be successful concordance of identification of ligamentum flavum and epidural space during a standard epidural procedure in pregnant patient. Secondary outcome will be successful concordance of identification of bony contact during a standard epidural procedure in pregnant patient.

Conditions

  • Epidural

Sponsors & Collaborators

  • Città di Roma Hospital

    lead OTHER

Principal Investigators

  • Giorgio Capogna · Citta di Roma Hospital

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-02
Primary Completion
2017-05-16
Completion
2017-05-20

More Related Trials

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 NCT03165708 on ClinicalTrials.gov