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COMPLETEDNCT02357953

Transpulmonary Thermodilution Using an Implented Central Venous Access Port

Perioperative hemodynamic optimization requires monitoring adapted to the risks of the surgery and the patient. The investigators currently use a local hemodynamic protocol based on the data of the li...

Lead sponsor: Gustave Roussy, Cancer Campus, Grand Paris•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Gustave Roussy, Cancer Campus, Grand Paris

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•presence of port
•scheduled surgery with perioperative optimization requirement according to the local hemodynamic protocol
•oral consent of the patient after oral and written information

Exclusion Criteria

•age inferior to 18
•Contraindication or failure to the insertion of the CVC
•Contraindication to the use of the port : local or general infection suspected or proved, absence of blood backflow

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: June 9, 2016Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment20

Start dateOct 2012

Last updatedJun 9, 2016

Condition

Medical Oncology

Locations shown

Gustave Roussy Cancer Campus Grand Paris

Villejuif, Val de Marne

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: June 9, 2016Data synced to Clareo: May 3, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions