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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 28 January 2013
Main ID:  NCT01064609
Date of registration: 05/02/2010
Primary sponsor: Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Public title: "Diagnostic Yield and Safety of Transbronchial Lung Biopsy Using Cryoprobes Versus Conventional Forceps.
Scientific title: "Diagnostic Yield and Safety of Transbronchial Lung Biopsy Using Cryoprobes Versus Conventional Forceps:a Randomized Clinical Trial"
Date of first enrolment: June 2011
Target sample size: 75
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT01064609
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic  
Countries of recruitment
Spain
Contacts
Name:   Alfons Torrego, Doctor
Address: 
Telephone:
Email:
Affiliation:  Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Name:   Mª Carmen Puzo, Doctor
Address: 
Telephone:
Email:
Affiliation:  Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Name:   Virginia Pajares, Doctor
Address: 
Telephone:
Email:
Affiliation:  Hospital del Santa Creu i Sant Pau
Key inclusion & exclusion criteria

Inclusion Criteria:

- Patients with Interstitial Lung disease.

Exclusion Criteria:

- Respiratory failure,haemodynamic instability, haemoptysis.



Age minimum: 18 Years
Age maximum: 80 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Interstitial Lung Disease
Intervention(s)
Procedure: Biopsy by cryoprobes
Procedure: Biopsy with conventional forceps
Primary Outcome(s)
To analyze the histological quality and immunohistochemical findings of samples obtained by cryoprobe compared with TBLB obtained by conventional forceps. [Time Frame: 3 years]
Secondary Outcome(s)
Secondary ID(s)
2008-003232-38
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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