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A Randomized Controlled Trial Comparing Percutaneous CT-Guided Biopsy and Shape-Sensing Robotic-Assisted Bronchoscopy

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NCT07761351 · readout in 620 d

Sponsored by Intuitive Surgical (industry) · ISRG — their whole pipeline →.

Phase
Phase 4
Status
Not yet recruiting
Study type
Interventional
Design
Randomized · None · Diagnostic
Enrollment
550estimated

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-08-31estimatedWhen the study began enrolling
Primary completion2028-04-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-04-30estimatedThe whole study's end, after follow-up
First posted2026-08-12actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Lung Cancer (Diagnosis)
  • Lung Nodule

Interventions

  • Procedure: Shape-Sensing Robotic-Assisted Bronchoscopy with Cone-Beam CT (ssRAB with CBCT) — also filed as ssRAB, Ion endoluminal system
  • Procedure: CT-guided percutaneous lung nodule biopsy — also filed as Transthoracic Needle Aspiration (TTNA), Transthoracic Needle Biopsy (TTNB)

Primary outcomes

what the primary-completion date above is the date OF
Diagnostic Efficacy of the Assigned Biopsy Procedure
measured At the index procedure
Peri-Procedural Pneumothorax Rate
measured From procedure to 7 days (or until subsequent intervention, whichever occurs first).

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