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Bronchoscopy
Robotic vs Electromagnetic Bronchoscopy for Lung Lesions (RELIANT Trial)
N/A
Waitlist Available
Led By Fabien Maldonado, MD, MSc
Research Sponsored by Vanderbilt University Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up duration of procedure, approximately 60 minutes
Awards & highlights
RELIANT Trial Summary
This trial compares two methods of bronchoscopy to diagnose lung lesions. It will help determine which is best.
Who is the study for?
The RELIANT Trial is for adults over 18 who are scheduled to undergo bronchoscopy to evaluate peripheral pulmonary lesions. It's not open to those already in a study requiring the use of either ILLUMISITE™ or Ion™ systems.Check my eligibility
What is being tested?
This trial compares two types of bronchoscopy: electromagnetic navigation (EMN) using the ILLUMISITE™ Platform and robotic-assisted bronchoscopy with the Ion™ Endoluminal System, focusing on their effectiveness in diagnosing lung abnormalities.See study design
What are the potential side effects?
Potential side effects may include discomfort at the procedure site, bleeding, infection risk from the instruments used, and possible complications related to lung tissue sampling.
RELIANT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ duration of procedure, approximately 60 minutes
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~duration of procedure, approximately 60 minutes
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Diagnostic yield, defined as the proportion of procedures that results in acquisition of lesional tissue. Lesional tissue is defined by the presence of histopathological findings that readily explain the presence of a pulmonary lesion.
Secondary outcome measures
Duration of procedure
RELIANT Trial Design
2Treatment groups
Active Control
Group I: Ion™ Endoluminal System (SSCB bronchoscopy)Active Control1 Intervention
Participants in the Ion™ Endoluminal System arm will undergo a diagnostic bronchoscopy with the Ion™ Endoluminal System (SSCB) machine.
Group II: ILLUMISITE™ Platform (EMN bronchoscopy)Active Control1 Intervention
Participants in the ILLUMISITE™ Platform arm will undergo a diagnostic bronchoscopy with the ILLUMISITE™ Platform (EMN) machine.
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Who is running the clinical trial?
Vanderbilt University Medical CenterLead Sponsor
857 Previous Clinical Trials
671,780 Total Patients Enrolled
Fabien Maldonado, MD, MScPrincipal InvestigatorVanderbilt University Medical Center
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I choose not to participate in the trial.I am 18 years old or older.I am scheduled for a lung scan using a special camera.
Research Study Groups:
This trial has the following groups:- Group 1: Ion™ Endoluminal System (SSCB bronchoscopy)
- Group 2: ILLUMISITE™ Platform (EMN bronchoscopy)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any vacancies still available for participants in this experiment?
"The clinical trial described is no longer recruiting, as indicated by the data on clincialtrials.gov. The study was launched July 1st 2023 and last updated January 30th 2023; however, other trials are still actively accepting patients at present."
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