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NCT01115309 · ClinicalTrials.gov registry record · NA
XprESS Registry Study
A NA study, sponsored by Entellus Medical.
- Completed
- Registry status
- NA
- Development phase
- 175
- Enrollment target
NCT01115309: Completed NA study, sponsored by Entellus Medical.
NCT01115309 is a NA study that has completed, run by Entellus Medical. The registered enrollment target is 175 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01115309, a NA study, has completed, sponsored by Entellus Medical.
- COMPLETED
- Registry status
- NA
- Development phase
- 175 participants
- Enrollment target
Study Summary
This is a prospective, non-randomized, multi-center study to assess safety and long-term patency of the ostia treated with the XprESS device per the device indication for use (IFU).
Primary Outcome
Adverse event reporting as related to XprESS device or procedure
Interventions
- DEVICE XprESS Balloon Device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 175 participants |
| Start Date | 2010-04 |
| Est. Completion | 2011-12 |
| Phase | NA |
What the finished NCT01115309 record still lists
NCT01115309 is an interventional study that assigns participants to a tested intervention. The registered 175 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower).
The record links to 0 conditions, and to 1 intervention - of which XprESS Balloon Device is the first listed.
NCT01115309 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01115309 about?
NCT01115309 is a clinical study titled "XprESS Registry Study". This is a prospective, non-randomized, multi-center study to assess safety and long-term patency of the ostia treated with the XprESS device per the device indication for use (IFU).
What is the current status of trial NCT01115309?
This trial is currently completed. It is a NA study. The enrollment target is 175 participants. The study started on 2010-04. Estimated completion is 2011-12.
What interventions are being tested in trial NCT01115309?
The interventions under investigation include: XprESS Balloon Device (DEVICE).
Who is sponsoring clinical trial NCT01115309?
This trial is sponsored by Entellus Medical, which has 11 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01115309's enrollment target sits among peer trials
175 610th of 2000 higher than 1,391 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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