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Suitability of PICC for Transpulmonary Thermodilution Compared to CICC

Are Peripherally Inserted Central Catheters (PICC) Suitable for Cardiac Output Assessment With Trans-pulmonary Thermodilution

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03834675
Enrollment
20
Registered
2019-02-08
Start date
2018-06-01
Completion date
2019-01-31
Last updated
2020-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CVC, Hemodynamic Monitoring, Peripherally Inserted Central Catheters, Transpulmonary Thermodilution

Keywords

PICC, shock, cardiac output

Brief 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 we try to assess their reliability for measuring cardiac index (CI) with trans-pulmonary thermodilution (TPTD) technique.

Interventions

Thermodilution was attempted via PICC and via CICC

Sponsors

Claudio Sandroni
CollaboratorUNKNOWN
Sofia Cacciola
CollaboratorUNKNOWN
Antonio Maria Dell Anna
CollaboratorUNKNOWN
Mauro Pittiruti
CollaboratorUNKNOWN
Maria Giuseppina Annetta
CollaboratorUNKNOWN
Cesare Colosimo
CollaboratorUNKNOWN
Massimo Antonelli
CollaboratorUNKNOWN
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult patients (≥18 years) admitted to the ICU * Patients requiring hemodynamic monitoring using EV1000TM * Patients having both PICC and CICC in place (these patients had their PICC replaced with a CICC, usually at the time of ICU admission, or vice versa, usually at the end of their ICU stay, and were enrolled immediately after the placement of the new device before the previous one was removed)

Exclusion criteria

* body weight \<40 kg * severe aortic regurgitation or intra-cardiac shunt * treatment with an intra-aortic balloon pump * contraindication for placement of PICC, CICC or a femoral arterial catheter * abdominal aneurism * extracorporeal circulation * pregnancy * lack of informed consent

Design outcomes

Primary

MeasureTime frameDescription
Cardiac Index comparison via PICCOne hourcomparison of hemodynamic measurements made by the TPTD from the VolumeView/EV1000TM system via PICC vs. CICC.

Secondary

MeasureTime frameDescription
Comparison 4Fr PICCs to CICCone hourComparison of single-lumen 4 Fr PICCs to CICC in their reliability of assessing cardiac output
Comparison 5Fr PICCs to CICCone hourComparison of dual-lumen 5 Fr PICCs to CICC in their reliability of assessing cardiac output

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026