At a glance
ClinicalIndex Comparison RecordN/ACompleted· 23 enrolled
Drug / intervention
iNod Systemdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Feasibility Study of a Bronchoscopic Ultrasound-Guided Tissue Acquisition System With Real-time Visualization for Collection of Cytology Specimens of Peripheral Pulmonary Lesions
In Brief
A clinical study evaluating iNod System for Solitary Pulmonary Nodule and Biopsy, Fine-Needle. Completed, enrolled 23 participants across 3 sites.
Detailed Summary
The purpose of this study is to demonstrate feasibility to access, visualize, and obtain specimens adequate for cytology of lung lesions in subjects with suspected lung cancer when using the iNod System.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSolitary Pulmonary Nodule, Biopsy, Fine-Needle
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJul 2016
Enrollment StartJan 2017
Primary CompletionJun 2017
Study CompletionJun 2017
TodayJul 2026
First PostedJul 14, 2016
Enrollment StartJan 18, 2017
Primary CompletionJun 8, 2017
Study CompletionJun 14, 2017
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 10.0 years ago
Interventions
iNod Systemdevice
The iNod System is intended for use for diagnostic ultrasound imaging and ultrasound-guided fine needle aspiration (FNA) of extramural and submucosal lesions of the tracheobronchial tree.