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OpenTrials
Completed

NCT Number: NCT02787512

Preoperative Biliary Drainage With Metal Versus Plastic Stents in Periampullary Cancer

Currently, routine preoperative biliary drainage (PBD) was not recommended. However, PBD is still necessary in case of patients with cholangitis or very high level of bilirubin or patients who are expected to receive delayed surgery.

The aim of this clinical trial is to demonstrate non-inferiority of uncovered self-expandable metal stent to plastic stent for PBD by endoscopic retrograde cholangiopancreatography in patients with periampullary cancer undergoing curative intent pancreaticoduodenectomy.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, South Korea

Loading trial locations.

About this study

Jaundice is one of the most common symptoms in patients with periampullary cancers including pancreatic cancer, common bile duct (CBD) cancer, ampulla of Vater (AoV) cancer, and duodenal cancer. Traditionally, preoperative biliary drainage (PBD) was routinely performed in these cancers because it might favorably influence sepsis, endotoxemia, and intravascular coagulation. However, a recent randomized control study reported that routine PBD in patients undergoing surgery for cancer of the pancreatic head increases the rate of complications. Therefore, routine PBD was not recommended. However, PBD is still necessary in case of patients with cholangitis or very high level of bilirubin or patients who are expected to receive delayed surgery.

In these patients with necessity of PBD, a plastic stent (PS) has been used because it is good for temporary use with cheap prices. However, it is sometimes occluded before surgery or not enough for rapid decompressing jaundice mainly because of its short diameter. In this aspect, a self-expandable metal stent (SEMS) has strength compared to PS because it has a longer diameter which enables rapid decompression with a fewer events of occlusion. However, SEMS is much more expensive than PS and the exact length of stent is more critical.

Although there are still lack of evidence which compares the results between PS and SEMS, National Comprehensive Cancer Network (NCCN) guidelines recently recommended the use of a short SEMS for pancreatic adenocarcinoma patients with cholangitis or fever. However, we needed more concrete evidence about this principle.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

A. Patients 20-80 years old B. Patients with surgically resectable periampullary cancer on CT scans with or without MRI or PET-CT scans C. ECOG Performance score 0 or 1 D. Patients who need preoperative biliary drainage (PBD) because of one or more of following causes

  • Cholangitis defined as revised Tokyo guidelines
  • Level of total bilirubin >= 10mg/dL
  • Expected time to operation >= 7 days

Exclusion criteria

A. Patients who received previous endoscopic biliary drainage or percutaneous biliary drainage B. Patients with acute pancreatitis before PBD

C. Patients with bleeding tendency or coagulopathy or anticoagulation therapy as follows:

  • Patients who take clopidogrel within 5 days before PBD
  • Patients who take warfarin within 2 days before PBD
  • Patients who receive heparin within 1 days before PBD D. Patients with pregnancy or suspected pregnancy E. Patients who are currently enrolled in another investigational trials that would directly interfere with current study

Treatment and study plan

stent

Device

Endoscopic biliary stent insertion

Primary outcomes

  1. Reintervention rate until operation

    Time frame: Between preoperative biliary drainage and surgery

    Between preoperative biliary drainage and surgery, reintervention (re-preoperative biliary drainage) would be checked and analyzed.

Secondary outcomes

  1. Other complication rate associated with endoscopic stent insertion and stent indwell

    Time frame: Between preoperative biliary drainage and surgery

    Until surgery, preoperative biliary drainage associated with complication would be checked and analyzed.

  2. Rate of decrease of total bilirubin

    Time frame: Between preoperative biliary drainage and surgery

    Amount of decrease of total bilirubin between preoperative biliary drainage and surgery would be checked.

  3. Time to operation

    Time frame: Between preoperative biliary drainage and surgery

    Interval between preoperative biliary drainage and surgery would be checked.

  4. Time to hospital discharge after pancreaticoduodenectomy

    Time frame: 6 month

    Interval between surgery and discharge would be checked.

  5. Mortality until 3 months after pancreaticoduodenectomy

    Time frame: 3 month

    The mortality rate would be calculated

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Collaborators

  • Boston Scientific Corporation

Registry information

Official study title

A Randomized Controlled Trial for Preoperative Biliary Drainage With Metal Versus Plastic Stents in Patients With Periampullary Cancer

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Jun 1, 2016
Registry last updated
Feb 12, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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