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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01153074
Other study ID # USP01089/09-TBF
Secondary ID
Status Completed
Phase N/A
First received June 28, 2010
Last updated May 23, 2017
Start date June 2010
Est. completion date October 2016

Study information

Verified date May 2017
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the feasibility of closing bronchopleural fistulas with devices originally developed for correction of cardiac septal defects deployed through bronchoscopic procedures.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date October 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender All
Age group 14 Years and older
Eligibility Inclusion Criteria:

- Patients over 14 years old

- Bronchopleural fistulas

Exclusion Criteria:

- Clinical conditions increasing surgical risk (hemodynamic instability, respiratory distress)

- Immunosuppressed patients

- Acute intense inflammatory process in fistula edge

- Suppurative pleural cavity infection

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Closure of bronchopleural fistula with Occlutech Figulla
Patients with bronchopleural fistulas will be submitted to a bronchoscopic procedure to deploy the cardiac septal defect occluder in the fistula traject.

Locations

Country Name City State
Brazil Heart Institute (InCor) Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo Sao Paulo
Brazil Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo Sao Paulo

Sponsors (3)

Lead Sponsor Collaborator
University of Sao Paulo InCor Heart Institute, Occlutech International AB

Country where clinical trial is conducted

Brazil, 

References & Publications (4)

Scordamaglio PR, Tedde ML, Minamoto H, Assad RS, Fernandes PMP. Can total bronchopleural fistulas from complete stump dehiscence be endoscopically treated? Eur J Cardiothorac Surg. 2017 Apr 1;51(4):702-708. doi: 10.1093/ejcts/ezw377. — View Citation

Scordamaglio PR, Tedde ML, Minamoto H, Pedra CA, Jatene FB. Endoscopic treatment of tracheobronchial tree fistulas using atrial septal defect occluders: preliminary results. J Bras Pneumol. 2009 Nov;35(11):1156-60. English, Portuguese. — View Citation

Tedde ML, Minamoto H, Scordamaglio PR, Rodrigues A, Moura EG, Pedra CA. Broncoscopic closure of tracheoesophageal fistulas. Ann Thorac Surg. 2011 Apr;91(4):1311. doi: 10.1016/j.athoracsur.2010.09.015. — View Citation

Tedde ML, Scordamaglio PR, Rodrigues A, Minamoto H, Alfinito FS. Minimally invasive closure of bronchopleural fistulas. Chest. 2011 Sep;140(3):826. doi: 10.1378/chest.11-0719. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Closure of tracheobronchial fistulas with the Occlutech Figulla ASD N occluder The closure of the fistulas will be bronchoscopically observed at regular intervals: one week, three weeks, two months and six months.
At the third months post intervention, a thorax CT scan will ascertain the correct position and stability of the device.
1 year
See also
  Status Clinical Trial Phase
Not yet recruiting NCT04435249 - ENgineered Tissue Repair of BronchopleUral fiSTula Phase 1/Phase 2
Recruiting NCT02961725 - Stem Cells for Treatment of Bronchopleural Fistula Phase 1
Completed NCT05304897 - PRP Efficacy and Safety in BPF N/A