Advanced Robotic Techniques and Rapid Onsite Evaluation for Minimally Invasive Diagnosis and Next-Generation Sequencing.
Starting soon · Not applicable
Conditions studied: Peripheral Pulmonary Lesions (PPLs)
In brief
ARTEMIS is a multicenter randomized controlled trial. The goal is to understand whether rapid onsite evaluation during robotic assisted bronchoscopy improves the diagnostic performance of the procedure or not.
Key facts
- Study ID
- NCT07685977
- Run by
- Vanderbilt University Medical Center
- People needed
- 400
- Starts
- 2026-10-01
- Expected to finish
- 2029-04-01
- Last updated by the study team
- 2026-07-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- ≥ 18 years of age at time of bronchoscopy
- Undergoing robotic assisted bronchoscopy to biopsy a pulmonary lesion
You may not qualify if…
- Declines to participate or inability to provide informed consent.
- Clinician determination that the use of ROSE is required or contraindicated for the optimal care of an individual patient
- Patient enrolled in another trial that requires ROSE for PPL biopsy
- Patient previously consented for this trial
- Pregnant or incarcerated patients
Where it is running
- Northwestern Memorial Hospital — Chicago, Illinois, United States
- Rush University Medical Center — Chicago, Illinois, United States
- Johns Hopkins University — Baltimore, Maryland, United States
- Lahey Hospital and Medical Center — Burlington, Massachusetts, United States
- Memorial Sloan Kettering Cancer Center — New York, New York, United States
- University of North Carolina Medical Center — Chapel Hill, North Carolina, United States
- Medical University of South Carolina — Charleston, South Carolina, United States
- Vanderbilt University Medical Center — Nashville, Tennessee, United States
Full record on ClinicalTrials.gov
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