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Status unknownNCT04911647Updated Jun 3, 2021

A Prospective Randomized Multi-center Study for Efficacy of Metallic Biliary Stent Compared to Plastic Stent in Patients Receiving Neoadjuvant Chemotherapy for Resectable Pancreatic Cancer

An interventional study of ERCP using plastic stent and ERCP using metal stent in Resectable Pancreatic Cancer With Biliary Obstruction, sponsored by Yonsei University. Status unknown at 1 site in Korea, Republic of. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2021-06-03.

Sponsored by Yonsei University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified May 2021), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
196
Allocation
Randomized
Ages
20 Years and older
Sex
All
01

Study summary

Pancreatic cancer is the eighth most common occurrence in Korea. In the United States, pancreatic cancer is expected to be the number two cause of death from cancer in 2030. The prevalence of pancreatic cancer is also on the rise in Korea. The 5-year survival rate of pancreatic cancer in Korea is 10.8%. According to the 2017 cause of death statistics, pancreatic cancer mortality is ranked fifth. It is known to have the worst prognosis of cancer in the body. The median survival period of unresectable pancreatic cancer is only six months, and resection is the only treatment that can be expected to be completely cured, but only about 10% of cases are possible to be operable at the time of diagnosis.

In the 2000s, the studies began to emerge on diagnosis and treatment of pancreatic cancer with intermediate anatomical and imaging characteristics of resectable and locally advanced pancreatic cancer. Margin negative resection plays an important role in the long-term survival rate in surgical treatment of pancreatic cancer. Prior to 2001, pancreatic cancer with invasion of vein was considered impossible to perform radical resection. However, the studies have been published that a satisfactory long-term survival rate and margin negative resection could be obtained when venous resection was performed along with radical resection. Since the 2006, the National Comprehensive Cancer Network (NCCN) guideline, after performing radical resection among locally advanced pancreatic cancers without remote metastasis, pancreatic cancers with high risk of margin positive resection and treatment failure were classified as "borderline resectable". In the borderline resectable pancreatic cancer, neoadjuvant therapy was recommended before surgery. In recent years, the neoadjuvant therapy has been reported to raise the survival rate in resectable pancreatic cancer. Furthermore, a prospective study is in progress to demonstrate the effectiveness of neoadjuvant therapy with FOLFIRINOX in resectable pancreatic cancer. If pancreatic cancer is located in the head of pancreas, jaundice can be occurred often. In the case of preoperative jaundice, the possibility of postoperative complications increases. So biliary drainage is performed before surgery. In biliary drainage, usually the plastic stent was inserted through the endoscope. If the metal stent is inserted in the biliary obstruction, it can cause severe inflammation around the bile duct due to the radial force, and it is difficult to remove in the surgery. However, the meta-analysis comparing the groups of metal and plastic stents in the recent preoperative biliary drainage showed no difference of postoperative complication, and postoperative pancreatic fistula was lower in the group of metal stents (5.1% vs. 11.8% p=0.04). In addition, fewer re-intervention cases before surgery were found in the group of metal stents (3.4% vs.14.8% p \< 0.0001).

Not only in the borderline resectable, but also in the resectable pancreatic cancer, neoadjuvant therapy has recently been actively performed in the cases of large tumor size, high CA 19-9, large lymph nodes, severe weight loss, and severe pain. The comparison study of the efficacy between plastic and metal stents in preoperative bile drainage in pancreatic cancer with neoadjuvant therapy has not yet been prospectively performed. However, retrospective studies have shown that metal stents have a lower re-treatment rate than plastic stent (0.24 vs 0.54), and that there is no difference in post-operative complications. Therefore, we planned the study to compare the efficacy and safety between metal and plastic stent in biliary drainage performed in patients undergoing neoadjuvant therapy with pancreatic cancer.

02

Conditions studied

  • Resectable Pancreatic Cancer With Biliary Obstruction
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In context

Pancreatic Neoplasms

3,235 studies on the registry are indexed under Pancreatic Neoplasms; 899 are open to participants now.

This study's planned enrollment of 196 is above the median of 46 across 2,424 interventional studies indexed under Pancreatic Neoplasms.

Browse Pancreatic Neoplasms studies →

Lead sponsor

Yonsei University is the lead sponsor of 1,387 studies on the registry; 232 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patients aged 20 years or older who have confirmed histologically or radiologically resectable pancreatic cancer
  2. Patients with clinical obstruction symptoms and radiographically confirmed biliary obstruction related to malignant tumors
  3. Patients receiving neoadjuvant chemotherapy before surgery

Exclusion criteria

Exclusion Criteria:

  1. Patients diagnosed as unresectable pancreatic cancer
  2. Patients with biliary obstruction due to biliary cancer, not pancreatic cancer
  3. Patients with duodenal obstruction
  4. Patients with pancreatic cance and other cancers
  5. Patients with severe uncontrolled infection
  6. Patients with 3 or higher of performance score as the Eastern Cooperative Oncology Group
  7. Patients who have not agreed with the informed consent
  8. Patients who are technically unable to be undergone endoscopic procedures
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
196 participants (estimated)

Study arms

  • Active comparator
    The Plastic stent

    Patient group with plastic stent inserted in biliary obstruction through endoscope

    Device: ERCP using plastic stent

  • Experimental
    The metal stent

    Patient group with metal stent inserted in biliary obstruction through endoscope

    Device: ERCP using metal stent

Interventions

  • DeviceERCP using plastic stent

    Insertion of plastic stent (plastic stent with inner diameter 1.8mm or more) in the biliary obstruction will be performed using ERCP in the patients with the pancreatic cancer undergoing neoadjuvant therapy.

  • DeviceERCP using metal stent

    Insertion of metal stent (full covered self-expandable metal stent) in the biliary obstruction will be performed using ERCP in the patients with the pancreatic cancer undergoing neoadjuvant therapy.

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What researchers measure

Primary outcomes

  1. Re-intervention rate

    Re-intervention because of obstructive jaundice, cholangitis, stent malfunction, complication of procedure of ERCP

    Time frame: 6 months

Secondary outcomes

  1. Procedure related complication, Postoperative complication

    1. Complication because of procedure (ERCP) 2. Complication because of surgery

    Time frame: 6 months

07

Study locations

1 site
  • Severance Hospital, Yonsei University Health System
    Seoul, Korea, Republic of
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 3, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04911647
Lead sponsor
Yonsei University
Responsible party
Sponsor
First posted
Jun 3, 2021
Start date
Jun 2021 (estimated)
Primary completion
Jun 2022 (estimated)
Completion
Jun 2023 (estimated)
Last update
Jun 3, 2021

Study contacts

Seung Min Bang
Contact
bang7028@yuhs.ac
82-2-2228-1995
Seung Min Bang
principal investigator · Severance Hospital, Yonsei University Health System

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in May 2021. You cannot join it, but the record below documents what was studied.

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