Thin EBUS Pilot Study
Completed
Conditions studied: Lung; Node
In brief
This is a single-center pilot study at the Medical University of South Carolina (MUSC) to evaluate the safety and efficacy of the TCP-EBUS scope (Thin EBUS). This study will consist of a standard of care bronchoscopy and will be followed for approximately 3 months. While the device is not FDA approved, it is the same technology but a thinner version of the SCP-EBUS bronchoscope.
Key facts
- Study ID
- NCT04745962
- Run by
- Medical University of South Carolina
- People needed
- 51
- Starts
- 2020-09-09
- Expected to finish
- 2024-09-28
- Last updated by the study team
- 2026-02-02
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Willing and able to provide informed consent.
- >21 years of age or older.
- Target lesion(s) within the middle third of the lung, which will be determined radiographically prior to scheduling the procedure by the bronchoscopist or radiologist, or by being located at least 2 airway generations from the main carina as seen radiographically.
- Target lesion(s) location documented on CT scan report.
- Indicated for bronchosocpy.
- Bronchoscopic procedure scheduled within 30 days of the CT scan report.
You may not qualify if…
- Not suitable for flexible bronchoscopy as determined by the treating physician prior to the procedure.
- Currently on anticoagulation medications with INR >1.5.
- Currently using DOAC and does not suspend use at least 7 days prior to the index procedure
- Currently using Plavix and does not suspend use for at least 7 days prior to the index procedure.
Where it is running
- Medical University of South Carolina — Charleston, South Carolina, United States
Full record on ClinicalTrials.gov
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