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Measurement of Lung Water by Transpulmonary Thermodilution in Lung Transplanted Patients (PICCO-LungT)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00834054
First Posted: February 3, 2009
Last Update Posted: September 23, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Hopital Foch
  Purpose
Repeated measurements of lung water by single transpulmonary thermodilution during the first postoperative days following lung transplantation

Condition Intervention
Mucoviscidosis Pulmonary Insufficiency Procedure: Double-lung transplantation

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Interest of Repeated Extravascular Lung Water Measurements With the PICCO Device in Lung Transplanted Patients

Resource links provided by NLM:


Further study details as provided by Hopital Foch:

Primary Outcome Measures:
  • extra-vascular lung water [ Time Frame: first postoperative days ]

Secondary Outcome Measures:
  • pulmonary permeability index [ Time Frame: first postoperative days ]

Estimated Enrollment: 15
Study Start Date: January 2009
Study Completion Date: July 2011
Primary Completion Date: July 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Double-lung transplanted patients Procedure: Double-lung transplantation
Double-lung transplanted patients

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
double-lung transplanted patients
Criteria

Inclusion Criteria:

  • double-lung transplanted patients

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00834054


Locations
France
Hopital Foch
Suresnes, France, 92150
Sponsors and Collaborators
Hopital Foch
Investigators
Study Chair: Charles Cerf, MD Hopital Foch
  More Information

Responsible Party: Hopital Foch
ClinicalTrials.gov Identifier: NCT00834054     History of Changes
Other Study ID Numbers: 2008/18
First Submitted: February 2, 2009
First Posted: February 3, 2009
Last Update Posted: September 23, 2016
Last Verified: September 2016

Additional relevant MeSH terms:
Cystic Fibrosis
Pancreatic Diseases
Digestive System Diseases
Lung Diseases
Respiratory Tract Diseases
Genetic Diseases, Inborn
Infant, Newborn, Diseases