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RCT Comparing 19Ga vs 22Ga EBUS-TBNA Needles in Carcinoma.

Primary Purpose

Lung Neoplasm

Status
Unknown status
Phase
Phase 3
Locations
Belgium
Study Type
Interventional
Intervention
EBUS-TBNA needle
Sponsored by
KU Leuven
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Lung Neoplasm focused on measuring EBUS-TBNA

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • (suspected) stage IV lung carcinoma identified on spiral computed tomography scan
  • requiring an EBUS-TBNA investigation to obtain intrathoracic hilar or mediastinal lymph node tissue for diagnosis

Exclusion Criteria:

  • uncontrolled coagulopathy
  • tracheal stenosis

Sites / Locations

  • University Hospitals KU LeuvenRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

19 Ga EBUS-TBNA needle

22 Ga EBUS-TBNA needle

Arm Description

needle aspiration by a flexible 19 Ga needle (Olympus)

needle aspiration by a 22 Ga needle (Olympus)

Outcomes

Primary Outcome Measures

Tissue core
Descriptive tissue characteristics of tumor sample

Secondary Outcome Measures

Tumor cellularity per area of diagnostic tissue
Objective pathologic measurement of tumor density
Quantity of DNA extracted
Objective measurement of the amount of DNA
Success rate of Next Generation Sequencing
Feasibility of NGS testing

Full Information

First Posted
May 27, 2016
Last Updated
September 19, 2016
Sponsor
KU Leuven
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1. Study Identification

Unique Protocol Identification Number
NCT02906280
Brief Title
RCT Comparing 19Ga vs 22Ga EBUS-TBNA Needles in Carcinoma.
Official Title
Randomized Controlled Trial Comparing the Performance of 19 Gauge Versus 22 Gauge EBUS-TBNA Needles in Lung Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Unknown status
Study Start Date
May 2016 (undefined)
Primary Completion Date
July 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
KU Leuven

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
EBUS-TBNA is often the sole diagnostic test applied in patients with stage IV lung cancer. A limitation of the TBNA needle when using a 22 Gauge needle is the limited ability to procure adequate histological samples. Although a larger 19 Ga needle can procure histological samples as demonstrated by the conventional 19 Ga needle, published data are not existing with respect to molecular diagnostics. A new nitinol-based 19 Ga needle has been developed for EBUS-TBNA. Given the frequent usage of 22 Ga needles for molecular diagnostics and the recent technical advancements in 19 Ga needle technology, we conduct a RCT to compare the performance of both needle types.
Detailed Description
All patients with (suspected) stage IV lung carcinoma identified on spiral computed tomography scan and requiring an EBUS-TBNA investigation to obtain intrathoracic hilar or mediastinal lymph node tissue for diagnosis, subtyping and genotyping of lung cancer are eligible for participation in this study. Procedural technique : patients undergo an EBUS-TBNA procedure with either the Flex 19 Ga needle or the 22 Ga needle ; all procedures are performed using a linear array echoendosope under moderate sedation (standard practice). Primary endpoint of the study is the presence of core tissue that is defined as a continuous string of material as observed on the microscopic examination. Secondary endpoints are elements relevant to molecular analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Neoplasm
Keywords
EBUS-TBNA

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
78 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
19 Ga EBUS-TBNA needle
Arm Type
Experimental
Arm Description
needle aspiration by a flexible 19 Ga needle (Olympus)
Arm Title
22 Ga EBUS-TBNA needle
Arm Type
Active Comparator
Arm Description
needle aspiration by a 22 Ga needle (Olympus)
Intervention Type
Device
Intervention Name(s)
EBUS-TBNA needle
Intervention Description
tissue sampling
Primary Outcome Measure Information:
Title
Tissue core
Description
Descriptive tissue characteristics of tumor sample
Time Frame
14 months
Secondary Outcome Measure Information:
Title
Tumor cellularity per area of diagnostic tissue
Description
Objective pathologic measurement of tumor density
Time Frame
14 months
Title
Quantity of DNA extracted
Description
Objective measurement of the amount of DNA
Time Frame
14 months
Title
Success rate of Next Generation Sequencing
Description
Feasibility of NGS testing
Time Frame
14 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: (suspected) stage IV lung carcinoma identified on spiral computed tomography scan requiring an EBUS-TBNA investigation to obtain intrathoracic hilar or mediastinal lymph node tissue for diagnosis Exclusion Criteria: uncontrolled coagulopathy tracheal stenosis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christophe Dooms
Email
christophe.dooms@uzleuven.be
Facility Information:
Facility Name
University Hospitals KU Leuven
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marc Decramer
Email
marc.decramer@uzleuven.be
First Name & Middle Initial & Last Name & Degree
Christophe Dooms

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

RCT Comparing 19Ga vs 22Ga EBUS-TBNA Needles in Carcinoma.

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