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Epidural Catheter Location by Epidural Pressure Waveform

NCT04205773 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2019-12-20

No results posted yet for this study

Summary

The aim of this preliminary study was to evaluate the new CompuFlo instrument which allows pulsatile waveform recordings.

Conditions

  • Anesthesia, Local

Interventions

DEVICE

CompuFlo

After priming with 5 mL saline, the catheter was connected to CompuFlo to record the occurrence of pulsatile waveforms and/or their disappearance during its removal

Sponsors & Collaborators

  • European e-Learning School in Obstetric Anesthesia

    lead OTHER

Principal Investigators

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

Eligibility

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

Timeline & Regulatory

Start
2019-11-01
Primary Completion
2019-11-29
Completion
2019-11-30

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 NCT04205773 on ClinicalTrials.gov