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RECRUITING

Real World Registry for Use of the Ion Endoluminal System

NCT06004440 · View on ClinicalTrials.gov ↗

Study Summary

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.

Interventions

  • DEVICE Ion Endoluminal System

Study Locations (16)

North Carolina

  • Atrium Health of the Carolinas — Charlotte
  • Cone Health Moses Cone Memorial Hospital — Greensboro
  • FirstHealth Moore Regional Hospital — Pinehurst

Illinois

  • Ascension Alexian Brothers — Elk Grove Village
  • Blessing Hospital — Quincy

Florida

  • Orlando Health Orlando Regional Medical Center — Orlando

Kansas

  • Kansas University Medical Center — Kansas City

Louisiana

  • Tulane University — New Orleans

Michigan

  • Henry Ford Hospital — Detroit

Minnesota

  • Mayo Clinic — Rochester

New York

  • Mercy Hospital of Buffalo — Buffalo

Trial Details

FieldValue
Enrollment Target 3,000 participants
Start Date 2023-09-21
Est. Completion 2030-08

Sponsor

Intuitive Surgical

53 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06004440

The ClinicalTrials.gov registry entry for NCT06004440 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 3,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Intuitive Surgical, which has 53 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 9 conditions, with Lung Cancer appearing as the primary indexed condition, and to 1 intervention — of which Ion Endoluminal System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06004440 reports 16 study locations spanning 13 distinct geographic areas — top geographies include North Carolina, Illinois, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06004440 about?

NCT06004440 is a clinical study titled "Real World Registry for Use of the Ion Endoluminal System". 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.

What is the current status of trial NCT06004440?

This trial is currently recruiting. The enrollment target is 3,000 participants. The study started on 2023-09-21. Estimated completion is 2030-08.

What conditions does trial NCT06004440 study?

This clinical trial studies the following conditions: Lung Cancer, Neoplasms, Lung Diseases, Lung Neoplasms, Neoplasms by Site. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06004440?

The interventions under investigation include: Ion Endoluminal System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06004440?

This trial is sponsored by Intuitive Surgical, which has 53 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06004440 being conducted?

This trial has 16 study locations across Florida, Illinois, Kansas, Louisiana, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial