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TerminatedNCT02460120EASTUpdated Jan 27, 2017

Evaluation of the Archimedes™ System for Transparenchymal Nodule Access

An interventional study of Archimedes System in Lung Cancer, sponsored by Broncus Medical Inc. Terminated at 1 site in United States. Open to participants aged 21 Years to 75 Years. Per ClinicalTrials.gov, last updated 2017-01-27.

Sponsored by Broncus Medical Inc · Not applicable, Interventional, and Diagnostic

Why this study was terminated
Updates to device
Phase
Not applicable
Study type
Interventional
Enrollment
9
Allocation
Not applicable
Ages
21 Years to 75 Years
Sex
All
01

Study summary

The Archimedes System is an image-guided navigation system used to access tissue samples in the lungs. This study is being conducted to confirm the performance of the Archimedes System in patients who are scheduled for standard bronchoscopy to diagnose highly suspicious lung cancer or metastatic disease. Navigation to and sampling of the patient's lung cancer tumor is conducted.

02

Conditions studied

  • Lung Cancer
03

Who can participate

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

Inclusion criteria

  1. Age 21-75 years at screening
  2. Highly suspicious SPN, defined as distinct nodule with a diameter of ≥8mm 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:

    • Untreatable life-threatening arrhythmias
    • Inability to adequately oxygenate the patient during the procedure
    • Acute respiratory failure with hypercapnia (unless the patient is intubated and ventilated)
    • Recent myocardial infarction
    • Previously diagnosed high-grade tracheal obstruction
    • Uncorrectable coagulopathy
  2. Known coagulopathy
  3. Platelet dysfunction or platelet count \< 100 x 103 cells/mm3
  4. History of major bleeding with bronchoscopy
  5. Suspected pulmonary hypertension: additional testing required, such as echocardiogram
  6. Moderate-to-severe pulmonary fibrosis
  7. Severe emphysema or COPD: additional testing and PI consent is required
  8. Bullae >5 cm located in vicinity of target SPN
  9. Any other severe or life-threatening comorbidity that could increase the risk of bronchoscopic biopsy or ATV tunneling, for example:

    • ASA class > 3
    • > stage 3 heart failure
    • severe cachexia
    • severe respiratory insufficiency or hypoxia
  10. Ongoing systemic infection
  11. Contraindication to general anesthesia
  12. Inability to stop anticoagulants (e.g., heparin, Warfarin) or antiplatelet agents (e.g. aspirin, clopidogrel) prior to procedure
  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. Scheduled for lung surgery within 72hrs post-scheduled diagnostic bronchoscopy
  18. Pregnancy
04

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
9 participants (actual)

Study arms

  • Experimental
    Navigation and tissue sampling

    Guided bronchoscopic navigation and lung tissue sampling using the Archimedes System

    Device: Archimedes System

Interventions

  • DeviceArchimedes System

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

05

What researchers measure

Primary outcomes

  1. Proportion of biopsies yielding tissue sufficient for diagnosis

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

    Time frame: Up to 1 year

Secondary outcomes

  1. Procedure planning time

    The time from selecting the patient CT until the tunnel path has been selected, reviewed and exported.

    Time frame: Up to 1 year

  2. Nodule access time

    The time from the start of navigation until the sheath has been placed at the first biopsy target.

    Time frame: Up to 1 year

  3. Fluoroscopy time

    The total fluoroscopy time from the start of fused-fluoroscopic navigational guidance to the time the devices are removed from the point of entry.

    Time frame: Up to 1 year

  4. Patient registration time

    The total time it takes to correlate the patient's position via fluoroscopy with the navigational guidance system.

    Time frame: Up to 1 year

06

Study locations

1 site
  • Cancer Treatment Centers of America at Southwestern Regional Medical Center
    Tulsa, Oklahoma 74133, United States
07

Registry details

Key details

Study ID
NCT02460120
Lead sponsor
Broncus Medical Inc
Responsible party
Sponsor
First posted
Jun 2, 2015
Start date
Jul 2015
Primary completion
Dec 2015
Completion
Dec 2015
Last update
Jan 27, 2017

Study contacts

Daniel Nader, D.O.
principal investigator · Cancer Treatment Centers of America at Southwestern Regional Medical Center

Oversight

Data monitoring committee
No
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