ClinicalTrials.gg
TerminatedNCT02130128Updated Jun 8, 2015

Continuing Evaluation of the LungPoint ATV System

An interventional study of LungPoint ATV System in Lung Cancer, sponsored by Broncus Medical Inc. Terminated at 1 site in Germany. Open to participants aged 21 Years to 75 Years. Per ClinicalTrials.gov, last updated 2015-06-08.

Sponsored by Broncus Medical Inc · Not applicable and Interventional

Why this study was terminated
Sufficient clinical evidence was gathered
Phase
Not applicable
Study type
Interventional
Enrollment
6
Allocation
Not applicable
Ages
21 Years to 75 Years
Sex
All
01

Study summary

The purpose of this study is to evaluate the safety and performance of the LungPoint ATV System in patients who are scheduled for standard bronchoscopy to diagnose highly suspicious lung cancer.

Read the detailed description

The LungPoint ATV System is an image-guided navigation system used to access tissue samples in the lungs. This feasibility study is being conducted to assess the safety and yield of the LungPoint ATV System in patients who are scheduled for standard bronchoscopy to diagnose highly suspicious lung cancer. Navigation to and sampling of the patient's lung cancer tumor is conducted.

02

Conditions studied

  • Lung Cancer

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03

In context

Lung Neoplasms

7,334 studies on the registry are indexed under Lung Neoplasms; 1,555 are open to participants now.

This study's enrollment of 6 is below the median of 60 across 5,345 interventional studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

Broncus Medical Inc is the lead sponsor of 6 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Surgical candidates age 21-75 years at screening
  2. Highly suspicious SPN, defined as distinct nodule with a diameter of 10-30 mm in its largest dimension
  3. No known endobronchial tumor
  4. Tumor located anywhere in parenchymal tissue >1 cm from pleura and accessible bronchoscopically through a POE.
  5. Willing to participate in all aspects of study protocol for duration of study
  6. Able to understand study requirements
  7. Signs study-related informed consent document

Exclusion criteria

Exclusion Criteria:

  1. Any contraindication to bronchoscopy, for example: (a.) Untreatable life-threatening arrhythmias, (b.) Inability to adequately oxygenate the patient during the procedure, (c.) Acute respiratory failure with hypercapnia (unless the patient is intubated and ventilated), (d.) Recent myocardial infarction, (e.) Previously diagnosed high-grade tracheal obstruction, (f.) Uncorrectable coagulopathy.
  2. Known coagulopathy
  3. Platelet dysfunction or platelet count \< 100 x 103 cells/mm3
  4. History of major bleeding with bronchoscopy
  5. Pulmonary hypertension with mean PAP >25 mm
  6. Moderate-to-severe pulmonary fibrosis
  7. Moderate to severe emphysema or COPD with FEV1 \<60% predicted or RV >200% predicted
  8. Bullae >5 cm located in vicinity of target SPN or ATV tunnel
  9. Any other severe or life-threatening comorbidity that could increase the risk of bronchoscopic biopsy or ATV tunneling, for example: (a.) ASA class > 3, (b.) > stage 3 heart failure, (c.) severe cachexia, (d.) severe respiratory insufficiency or hypoxia
  10. Ongoing systemic infection
  11. Contraindication to general anesthesia
  12. Chronic use of anticoagulants (e.g., heparin, Warfarin) or antiplatelet agents (e.g. aspirin, clopidogrel)
  13. Participation in any other study in last 30 days
  14. Prior thoracic surgery on the same side of the lung as the SPN
  15. Breastfeeding women or females of childbearing potential with a positive pregnancy test prior to the procedure or the intent to become pregnant during the study.
  16. Life expectancy of less than one year.
  17. Patients with known intrapulmonary metastases of extrapulmonary cancer/tumors
  18. Scheduled for lung surgery within 7 days post-scheduled diagnostic bronchoscopy
05

Study design

Phase
Not applicable
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
6 participants (actual)

Study arms

  • Experimental
    Navigation and tissue sampling

    Guided bronchoscopic navigation and lung tissue sampling using the LungPoint ATV System

    Device: LungPoint ATV System

Interventions

  • DeviceLungPoint ATV System

    The LungPoint ATV System is an image-guided navigation system used to access tissue samples in the lungs.

06

What researchers measure

Primary outcomes

  1. Number of serious adverse events

    The number of serious adverse events (SAEs) rated as probably or definitely related to the study device and/or procedure divided by the number of patients in whom an attempt at study device use was made. This study protocol focuses specifically on sub-chronic pneumothorax, but will also track hemoptysis.

    Time frame: Up to 24 hours post procedure

Secondary outcomes

  1. Proportion of biopsies yielding tissue sufficient for diagnosis

    The number of nodules with at least one biopsy sufficient for a tissue diagnosis divided by the number of nodules sampled by the LP ATV System.

    Time frame: Upon asssessment of histology of tissue sample taken during procedure

07

Study locations

1 site
  • Thoraxklinik
    Heidelberg, 69126, Germany
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 8, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02130128
Lead sponsor
Broncus Medical Inc
Responsible party
Sponsor
First posted
May 5, 2014
Start date
Apr 2014
Primary completion
Dec 2014
Completion
Dec 2014
Last update
Jun 8, 2015

Study contacts

Felix Herth, MD
principal investigator · Heidelberg University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jun 2015. You cannot join it, but the record below documents what was studied.

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