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NCT06004440Active, not recruiting

Real World Registry for Use of the Ion Endoluminal System

A Multi-Center, Prospective, Single-Arm, Observational Study to Evaluate Real-World Outcomes for the Shape-Sensing Ion Endoluminal System

Source: ClinicalTrials.gov · Last updated 24 Apr 2026

Brief summary (registry, in English)

The primary objective of this study is to evaluate the performance of the Ion Endoluminal System with real-world use for pulmonary lesion localization or biopsy.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
1301 (actual)
First submitted
16 Aug 2023
Start date
Sept 2023
Primary completion date
Aug 2027
Lead sponsor
Intuitive Surgical
Diseases
Lung cancer
NCT number
NCT06004440

What you commit to

  • Study type: Observational
  • Participants enrolled: 1301
  • From Sept 2023 to the primary completion date, Aug 2027
  • 16 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subject is participating in an interventional research study or research study investigational agents with an unknown safety profile that would interfere with participation in this study.

Other

  • Subject is under the care of a Legally Authorized Representative (LAR) and is unable to provide informed consent on their own accord.
  • Female subjects who are pregnant or nursing at the time of the index bronchoscopy procedure, as determined by standard site practices.
  • Subjects that are incarcerated or institutionalized under court order, or other vulnerable populations.

Who the study is looking for

  • Subject is 18 years or older at the time of the index procedure.
  • Subject is a candidate for an elective, planned lung lesion localization or biopsy procedure utilizing the Ion Endoluminal System.
  • Subject able to understand and adhere to study requirements and provide informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (16)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mercy Hospital of Buffalo
Coordinator of this site? Confirm its status
BuffaloUnited StatesUnknown status
Atrium Health of the Carolinas
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CharlotteUnited StatesUnknown status
Ohio State University Wexner Medical Center
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ColumbusUnited StatesUnknown status
Henry Ford Hospital
Coordinator of this site? Confirm its status
DetroitUnited StatesUnknown status
Ascension Alexian Brothers
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Elk Grove VillageUnited StatesUnknown status
Cone Health Moses Cone Memorial Hospital
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GreensboroUnited StatesUnknown status
Kansas University Medical Center
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Kansas CityUnited StatesUnknown status
Aurora Medical Center Kenosha
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KenoshaUnited StatesUnknown status
Intermountain Medical Center
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MurrayUnited StatesUnknown status
Centennial Medical Center
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NashvilleUnited StatesUnknown status
Tulane University
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New OrleansUnited StatesUnknown status
Orlando Health Orlando Regional Medical Center
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OrlandoUnited StatesUnknown status
FirstHealth Moore Regional Hospital
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PinehurstUnited StatesUnknown status
Blessing Hospital
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QuincyUnited StatesUnknown status
Mayo Clinic
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RochesterUnited StatesUnknown status
Methodist Hospital
Coordinator of this site? Confirm its status
San AntonioUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.