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Main
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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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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28 January 2013 |
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Main ID: |
NCT01064609 |
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Date of registration:
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05/02/2010 |
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Primary sponsor: |
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Public title:
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"Diagnostic Yield and Safety of Transbronchial Lung Biopsy Using Cryoprobes Versus Conventional Forceps.
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Scientific title:
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"Diagnostic Yield and Safety of Transbronchial Lung Biopsy Using Cryoprobes Versus Conventional Forceps:a Randomized Clinical Trial" |
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Date of first enrolment:
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June 2011 |
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Target sample size:
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75 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01064609 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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Countries of recruitment
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Spain
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Contacts
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Name:
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Alfons Torrego, Doctor |
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Address:
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Telephone:
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Email:
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Affiliation:
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Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau |
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Name:
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Mª Carmen Puzo, Doctor |
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Address:
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Telephone:
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Email:
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Affiliation:
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Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau |
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Name:
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Virginia Pajares, Doctor |
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Address:
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Telephone:
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Email:
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Affiliation:
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Hospital del Santa Creu i Sant Pau |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients with Interstitial Lung disease.
Exclusion Criteria:
- Respiratory failure,haemodynamic instability, haemoptysis.
Age minimum:
18 Years
Age maximum:
80 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Interstitial Lung Disease
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Intervention(s)
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Procedure: Biopsy by cryoprobes
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Procedure: Biopsy with conventional forceps
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Primary Outcome(s)
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To analyze the histological quality and immunohistochemical findings of samples obtained by cryoprobe compared with TBLB obtained by conventional forceps.
[Time Frame: 3 years]
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Secondary ID(s)
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2008-003232-38
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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