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NCT01774019 · ClinicalTrials.gov registry record · NA
Preoperative Biliary Drainage in Resectable Pancreatic or Periampullary Cancer
A NA study, sponsored by Boston Scientific Corporation.
- Completed
- Registry status
- NA
- Development phase
- 284
- Enrollment target
NCT01774019: Completed NA study, sponsored by Boston Scientific Corporation.
NCT01774019 is a NA study that has completed, run by Boston Scientific Corporation. The registered enrollment target is 284 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01774019, a NA study, has completed, sponsored by Boston Scientific Corporation.
- COMPLETED
- Registry status
- NA
- Development phase
- 284 participants
- Enrollment target
Study Summary
The purpose of this study is to demonstrate that preoperative biliary drainage using self-expanding metal stents (SEMS) does not negatively impact overall surgical outcomes in patients undergoing pancreaticoduodenectomy for treatment of pancreatic or periampullary cancer.
Primary Outcome
The primary end point was all serious adverse events (SAEs), including all preoperative, operative and postoperative adverse events reported from the time of randomization to 120 days post-randomization or 30 days post-CIS (up to 150 days post-randomization), whichever occurred later.
Interventions
- DEVICE WallFlex™ Biliary RX Fully Covered/Uncovered Stent System
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 284 participants |
| Start Date | 2013-02-20 |
| Est. Completion | 2021-12-13 |
| Phase | NA |
What the finished NCT01774019 record still lists
NCT01774019 is an interventional study that assigns participants to a tested intervention. The registered 284 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 (80% lower).
The record links to 0 conditions, and to 1 intervention - of which WallFlex™ Biliary RX Fully Covered/Uncovered Stent System is the first listed.
NCT01774019 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01774019 about?
NCT01774019 is a clinical study titled "Preoperative Biliary Drainage in Resectable Pancreatic or Periampullary Cancer". The purpose of this study is to demonstrate that preoperative biliary drainage using self-expanding metal stents (SEMS) does not negatively impact overall surgical outcomes in patients undergoing pancreaticoduodenectomy for treatment of pancreatic or periampullary cancer.
What is the current status of trial NCT01774019?
This trial is currently completed. It is a NA study. The enrollment target is 284 participants. The study started on 2013-02-20. Estimated completion is 2021-12-13.
What interventions are being tested in trial NCT01774019?
The interventions under investigation include: WallFlex™ Biliary RX Fully Covered/Uncovered Stent System (DEVICE).
Who is sponsoring clinical trial NCT01774019?
This trial is sponsored by Boston Scientific Corporation, which has 280 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01774019's enrollment target sits among peer trials
284 377th of 2000 higher than 1,623 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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