Pilot Study of Navigational Bronchoscopy and Transthoracic Needle Biopsy
Primary Purpose
Peripheral Pulmonary Nodules
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Navigation guided bronchoscopy
Sponsored by
About this trial
This is an interventional diagnostic trial for Peripheral Pulmonary Nodules focused on measuring Lung nodule biopsy
Eligibility Criteria
Inclusion criteria:
- Target patient population: Patients with a peripheral pulmonary nodule as identified on CT chest ≤3cm from the pleura will be recruited. A PPN will be defined as a lesion >10mm and <3cm in diameter surrounded by lung parenchyma on CT chest. The decision for biopsy of the PPN will be made by the treating physician and agreed upon by the patient.
- Participants must be at least 18 years old or older
- No bleeding disorders
- Provide informed consent.
Exclusion criteria
- less than 18 years
- lack of fitness for flexible bronchoscopy as determined by the physician performing the bronchoscopy before the procedure
- inability to give informed consent
Sites / Locations
- Johns Hopkins University
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Assessing peripheral pulmonary nodules
Arm Description
To evaluate the feasibility and safety of a procedure path including convex Endobronchial Ultrasound (EBUS) lymph node sampling, navigation guided bronchoscopy (NB) and navigation guided transthoracic needle aspiration (N-TTNA).
Outcomes
Primary Outcome Measures
Feasibility
Feasibility assessed by number of participants with successful completion of biopsy (i.e. a biopsy was able to be obtained to collect a tissue sample)
Incidence of Pneumothorax
Presence of pneumothorax assessed in participants with successful completion of biopsy.
Secondary Outcome Measures
Positive Diagnostic Yield of Bronchoscopic Biopsy of Electromagnetic Guidance Trans-thoracic Needle Aspiration (ETTNA) Alone
Positive diagnostic yield of bronchoscopic biopsy of Electromagnetic Guidance Trans-thoracic Needle Aspiration (ETTNA) alone was defined by participants having benign or malignant pathology.
Positive Diagnostic Yield of Bronchoscopic Biopsy of ETTNA + EBUS + NB
Positive diagnostic yield of bronchoscopic biopsy of ETTNA + EBUS + NB was defined by participants having benign or malignant pathology.
Full Information
NCT ID
NCT02109458
First Posted
March 17, 2014
Last Updated
March 13, 2017
Sponsor
Johns Hopkins University
Collaborators
Veran Medical Technologies
1. Study Identification
Unique Protocol Identification Number
NCT02109458
Brief Title
Pilot Study of Navigational Bronchoscopy and Transthoracic Needle Biopsy
Official Title
Navigational Bronchoscopy and Transthoracic Needle Biopsy for the Diagnosis of Peripheral Pulmonary Nodules: A Safety and Feasibility Pilot
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
Veran Medical Technologies
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The goal of this study is to evaluate the feasibility and safety of navigation guided virtual transthoracic needle biopsy combined with navigational bronchoscopy for the diagnosis of peripheral pulmonary nodules (PPN).
Detailed Description
Accessing peripheral pulmonary nodules is problematic because they are often not visible endobronchially, not large enough to be visualized by x-ray fluoroscopy for transbronchial biopsy (TBBx), and/or do not lie within an accessible airway. In this study, investigators hope to evaluate new technologies to aid in PPN biopsy using navigation bronchoscopy (NB) combined with navigation transthoracic needle aspiration (N-TTNA) sampling of a PPN.
Patients meeting inclusion criteria who consent will undergo a convex Endobronchial Ultrasound (EBUS) bronchoscopy for evaluation and sampling of the mediastinum and hilum. Following this, NB will be performed with an ultrathin bronchoscope (4mm outer diameter with a 2 mm working channel) with R-EBUS and fluoroscopy. If the lesion is localized by NB and/or radial EBUS in conjunction with NB, TBBX will be taken. At the conclusion of TBBX sampling, a fluoroscopic evaluation to assess for the presence of pneumothorax will be performed and if one is present, appropriate clinical measures will be taken at the discretion of the treating team (tube thoracostomy, observation, etc.) and no further sampling techniques will be utilized. If the lesion was not able to be localized via NB and/or the physician feels insufficient sample was acquired for diagnosis and there is no evidence of pneumothorax, the patient will undergo N-TTNA at the same PPN during the same procedure time. It is envisioned that between 8-12 patients will require a N-TTNA to complete diagnosis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Pulmonary Nodules
Keywords
Lung nodule biopsy
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Assessing peripheral pulmonary nodules
Arm Type
Experimental
Arm Description
To evaluate the feasibility and safety of a procedure path including convex Endobronchial Ultrasound (EBUS) lymph node sampling, navigation guided bronchoscopy (NB) and navigation guided transthoracic needle aspiration (N-TTNA).
Intervention Type
Device
Intervention Name(s)
Navigation guided bronchoscopy
Intervention Description
Navigation guided transthoracic needle aspiration (N-TTNA) and navigation guided bronchoscopy (NB); guidance system is by Veran Medical Technologies, Inc.
Primary Outcome Measure Information:
Title
Feasibility
Description
Feasibility assessed by number of participants with successful completion of biopsy (i.e. a biopsy was able to be obtained to collect a tissue sample)
Time Frame
Immediately following procedure
Title
Incidence of Pneumothorax
Description
Presence of pneumothorax assessed in participants with successful completion of biopsy.
Time Frame
Immediately after procedure
Secondary Outcome Measure Information:
Title
Positive Diagnostic Yield of Bronchoscopic Biopsy of Electromagnetic Guidance Trans-thoracic Needle Aspiration (ETTNA) Alone
Description
Positive diagnostic yield of bronchoscopic biopsy of Electromagnetic Guidance Trans-thoracic Needle Aspiration (ETTNA) alone was defined by participants having benign or malignant pathology.
Time Frame
Approximately 1 week upon receipt of pathology report
Title
Positive Diagnostic Yield of Bronchoscopic Biopsy of ETTNA + EBUS + NB
Description
Positive diagnostic yield of bronchoscopic biopsy of ETTNA + EBUS + NB was defined by participants having benign or malignant pathology.
Time Frame
Approximately 1 week upon receipt of pathology report
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Target patient population: Patients with a peripheral pulmonary nodule as identified on CT chest ≤3cm from the pleura will be recruited. A PPN will be defined as a lesion >10mm and <3cm in diameter surrounded by lung parenchyma on CT chest. The decision for biopsy of the PPN will be made by the treating physician and agreed upon by the patient.
Participants must be at least 18 years old or older
No bleeding disorders
Provide informed consent.
Exclusion criteria
less than 18 years
lack of fitness for flexible bronchoscopy as determined by the physician performing the bronchoscopy before the procedure
inability to give informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lonny Yarmus, DO
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Pilot Study of Navigational Bronchoscopy and Transthoracic Needle Biopsy
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