Clinical Trials Directory

Trials / Completed

CompletedNCT01475084

Cryobiopsy or Forceps Biopsy During Semirigid Thoracoscopy: a Comparative Study

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
40 (actual)
Sponsor
The University Clinic of Pulmonary and Allergic Diseases Golnik · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare cryobiopsies with forceps biopsies during semirigid thoracoscopy.

Detailed description

The investigators are going to compare diagnostic yield and size, morphological features, immunohistochemistry as measures of the quality of the samples. The secondary aim is to evaluate safety with focus on bleeding intensity.

Conditions

Interventions

TypeNameDescription
DEVICEcryobiopsy (Autoclavable cryoprobe 20416-032 (ERBE, Germany) Flexible FB-55CD-1 Olympus forcepsThe tip of the cryoprobe will be attached to suspicious part of parietal pleura and activated by footswitch for 3 seconds. The frozen tissue is going to be extracted by gently pulling of the probe. The probe with the attached biopsy sample is going to be removed together with the thoracoscope through trocar. The biopsy sample will be released from the probe by thawing in the saline. Forceps biopsy will be performed on usual way.

Timeline

Start date
2011-11-01
Primary completion
2014-11-01
Completion
2014-11-01
First posted
2011-11-21
Last updated
2015-09-10

Locations

1 site across 1 country: Slovenia

Source: ClinicalTrials.gov record NCT01475084. Inclusion in this directory is not an endorsement.