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EBUS Guided Cryo Biopsy of Solitary Pulmonary Nodules

NCT01221493 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2010-10-15

No results posted yet for this study

Summary

To proof the feasibility and safety of EBUS guided transbronchial cryo biopsies in peripheral lung lesions

Conditions

  • Yield of Cryo Biopsy in Lung Cancer
  • Solitary Pulmonary Nodule

Interventions

PROCEDURE

Cryo biopsy

Cryoprobe, Erbe Company

Sponsors & Collaborators

  • Heidelberg University

    lead OTHER

Principal Investigators

  • Felix JF Herth, MD, PhD · Thoraxklinik, Universityof Heidelberg

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2010-12-31
Completion
2010-12-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01221493 on ClinicalTrials.gov