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Lung Transplantation for Pleuroparenchymal Fibroelastosis

Conditions
Fibroelastosis
Registration Number
NCT05044390
Lead Sponsor
Hospices Civils de Lyon
Brief Summary

This retrospective observational study will evaluate the outcomes of lung transplantation for a rare cause of interstitial lung disease called pleuroparenchymal fibroelastosis. Data will be collected from all transplantation center in France.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Lung transplantation (any type) for pleuroparenchymal fibroelastosis
  • Histologically confirmed pleuroparenchymal fibroelastosis on the recipient lungs
Exclusion Criteria
  • All other interstitial lung disease than pleuroparenchymal fibroelastosis
  • Pleuroparenchymal fibroelastosis who didn't underwent lung transplantation

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Post-operative mortalityAny death up to 90 days after lung transplantation

Any death after lung transplantation during the first 30 days or during the hospitalization following the lung transplantation (in-hospital mortality)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (4)

Marie Lannelongue Hospital

🇫🇷

Le Plessis-Robinson, France

Hopital Louis Pradel

🇫🇷

Lyon, France

Bichat Claude Bernard Hospital, APHP

🇫🇷

Paris, France

Foch Hospital

🇫🇷

Suresnes, France

Marie Lannelongue Hospital
🇫🇷Le Plessis-Robinson, France
: Elie FADEL : Elie FADEL, MD
Contact
33 1 40 94 28 00
e.fadel@ghpsj.fr

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