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NCT02028052 · ClinicalTrials.gov registry record · NA
Procedural Outcomes in Endobronchial Ultrasound - Transbronchial Needle Aspiration (EBUS-TBNA) With and Without Rapid On-Site Evaluation (ROSE)
A NA study, sponsored by Duke University.
- Terminated
- Registry status
- NA
- Development phase
- 37
- Enrollment target
NCT02028052: Clinical Trial NA study, sponsored by Duke University.
NCT02028052 is a NA study that was terminated before completion, run by Duke University. The registered enrollment target is 37 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02028052, a NA study, was terminated before completion, sponsored by Duke University.
- TERMINATED
- Registry status
- NA
- Development phase
- 37 participants
- Enrollment target
Study Summary
The objective of this study is comparing the attributable procedural time of Endobronchial Ultrasound - Transbronchial Needle Aspiration (EBUS-TBNA) when sampling mediastinal and hilar lymph nodes with or without Rapid On-Site Evaluation (ROSE). The primary outcome will be the time elapsed from EBUS bronchoscope insertion to bronchoscope withdrawal. Secondary outcomes will include total number of sampled lymph nodes, average number of needle aspirations per lymph node sampled, overall diagnostic yield, and procedural time of the cytopathologist.
Primary Outcome
The primary endpoint is the time elapsed from EBUS bronchoscope insertion to bronchoscope withdrawal.
Interventions
- PROCEDURE ROSE
- DEVICE 22 gauge Vizishot needles
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2012-04 |
| Est. Completion | 2014-11 |
| Phase | NA |
Why NCT02028052 stopped before completion
NCT02028052 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 2 interventions - of which ROSE is the first listed.
NCT02028052 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02028052 about?
NCT02028052 is a clinical study titled "Procedural Outcomes in Endobronchial Ultrasound - Transbronchial Needle Aspiration (EBUS-TBNA) With and Without Rapid On-Site Evaluation (ROSE)". The objective of this study is comparing the attributable procedural time of Endobronchial Ultrasound - Transbronchial Needle Aspiration (EBUS-TBNA) when sampling mediastinal and hilar lymph nodes with or without Rapid On-Site Evaluation (ROSE). The primary outcome will be the time elapsed from EBUS...
What is the current status of trial NCT02028052?
This trial is currently terminated. It is a NA study. The enrollment target is 37 participants. The study started on 2012-04. Estimated completion is 2014-11.
What interventions are being tested in trial NCT02028052?
The interventions under investigation include: ROSE (PROCEDURE), 22 gauge Vizishot needles (DEVICE).
Who is sponsoring clinical trial NCT02028052?
This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02028052's enrollment target sits among peer trials
37 1540th of 2000 higher than 460 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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
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