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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02611297
Other study ID # IIBSP-CRI-2013-142
Secondary ID
Status Recruiting
Phase N/A
First received May 21, 2015
Last updated November 19, 2015
Start date November 2013
Est. completion date December 2015

Study information

Verified date October 2015
Source Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Contact Virginia Pajares, MD, PhD
Phone +34935565972
Email vpajares@santpau.cat
Is FDA regulated No
Health authority Spain: Comité Ético de Investigación Clínica
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the the diagnostic yield and safety of transbronchial lung biopsies (TBLB) with cryoprobe in patients with mechanical ventilation.


Recruitment information / eligibility

Status Recruiting
Enrollment 15
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- =18 years old

- Patients with mechanical ventilation.

- Patients with diffuse lung disease of unknown etiology.

- Need for confirming/excluding a diagnosis, with therapeutical and prognosis implications.

- Inform consent signed by family.

Exclusion Criteria:

- Use of anticoagulant therapy or presence of a coagulation disorder (abnormal platelets counts, international normalized ratio > 1.5).

- Comorbidities that could increase the risk of the TBLB.

- Bullous emphysema.

- Hemoptysis, pneumothorax.

- Severe respiratory insufficiency requiring PEEP >12 cm H2O

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
Cryoprobe


Locations

Country Name City State
Spain Germans Tries i Pujol Hospital Badalona Barcelona
Spain Hospital Clinic de Barcelona Barcelona
Spain Hospital de la Santa Creu i Sant Pau Barcelona

Sponsors (3)

Lead Sponsor Collaborator
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau Germans Trias i Pujol Hospital, Hospital Clinic of Barcelona

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adverse events related to transbronchial lung biopsy (TBLB) with cryoprobe 27 months Yes
Secondary Diagnostic yield of transbronchial lung biopsy (TBLB) obtained by cryoprobes 27 months Yes
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