Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02111824 · ClinicalTrials.gov registry record · Phase 1

A Multimodality Image-guided System for Peripheral Lung Cancer Diagnosis and Therapy

A Phase 1 study, sponsored by The Methodist Hospital Research Institute.

Terminated
Registry status
Phase 1
Development phase
7
Enrollment target

NCT02111824: Clinical Trial Phase 1 study, sponsored by The Methodist Hospital Research Institute.

NCT02111824 is a Phase 1 study that was terminated before completion, run by The Methodist Hospital Research Institute. The registered enrollment target is 7 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02111824, a Phase 1 study, was terminated before completion, sponsored by The Methodist Hospital Research Institute.

TERMINATED
Registry status
Phase 1
Development phase
7 participants
Enrollment target

Study Summary

The goal of this clinical research study is to test the use of a minimally invasive multimodality image-guided (MIMIG) intervention system used for performing a lung biopsy. The safety of the MIMIG intervention system will also be studied.

Primary Outcome

Technical success rate of completing the biopsy procedure using the MIMIG system with and without fiber-optical imaging measured where technical success is defined as the ability to use the navigational components of the MIMIG system to obtain a tissue specimen from a lung nodule; ability to use the navigational components of the system during the biopsy procedure, the ability to successfully perform optical imaging of the lung nodule and the ability to obtain a tissue specimen from the lung nod

Interventions

  • DRUG Indocyanine Green (ICG)
  • DEVICE MIMIG System

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2014-01-05
Est. Completion 2019-11
Phase Phase 1

Why NCT02111824 stopped before completion

NCT02111824 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (88% lower).

The record links to 0 conditions, and to 2 interventions - of which Indocyanine Green (ICG) is the first listed.

NCT02111824 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02111824 about?

NCT02111824 is a clinical study titled "A Multimodality Image-guided System for Peripheral Lung Cancer Diagnosis and Therapy". The goal of this clinical research study is to test the use of a minimally invasive multimodality image-guided (MIMIG) intervention system used for performing a lung biopsy. The safety of the MIMIG intervention system will also be studied.

What is the current status of trial NCT02111824?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 7 participants. The study started on 2014-01-05. Estimated completion is 2019-11.

What interventions are being tested in trial NCT02111824?

The interventions under investigation include: Indocyanine Green (ICG) (DRUG), MIMIG System (DEVICE).

Who is sponsoring clinical trial NCT02111824?

This trial is sponsored by The Methodist Hospital Research Institute, which has 126 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02111824's enrollment target sits among peer trials

7 1972nd of 2000 higher than 27 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02111824, the US trial registry maintained by the National Library of Medicine. NCT02111824 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.