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Single-lumen 5Fr and Triple-lumen 6Fr PICCs Are Accurate for Hemodynamic Measurement by Transpulmonary Thermodilution.

NCT04241926 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2020-07-23

No results posted yet for this study

Summary

Peripherally inserted central catheters (PICCs) are increasingly used in intensive care unit (ICU) as an alternative to centrally inserted central catheters (CICCs) for intravenous infusion. In the present study the investigators try to assess their reliability for measuring cardiac index (CI) with trans-pulmonary thermodilution (TPTD) technique.

Conditions

  • Peripherally Inserted Central Catheters
  • Centrally Inserted Central Catheter
  • Transpulmonary Thermodilution
  • Hemodynamic Monitoring

Interventions

DIAGNOSTIC_TEST

transpolmonary thermodilution

Thermodilution was attempted via PICC and via CICC in the same patient

Sponsors & Collaborators

  • Antonio Maria Dell Anna

    collaborator UNKNOWN

  • Sofia Cacciola

    collaborator UNKNOWN

  • Claudio Sandroni

    collaborator UNKNOWN

  • Giulia Chiuri

    collaborator UNKNOWN

  • Mauro Pittiruti

    collaborator UNKNOWN

  • Cesare Colosimo

    collaborator UNKNOWN

  • Maria Giuseppina Annetta

    collaborator UNKNOWN

  • Massimo Antonelli

    collaborator UNKNOWN

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

    lead OTHER

Principal Investigators

  • Massimo Antonelli, MD · Università Cattolica del sacro Cuore- Fondazione Policlinico Universitario A. Gemelli IRCSS

Study Design

Purpose
OTHER
Masking
SINGLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2019-05-01
Primary Completion
2020-02-09
Completion
2020-02-29

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 NCT04241926 on ClinicalTrials.gov