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

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006294

Enrollment

196

Registered

2021-06-24

Start date

2021-06-07

Completion date

Unknown

Last updated

2021-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Procedure/Surgery : It is targeted at patients with biliary obstruction and resectable pancreatic cancer undergoing neoadjuvant chemotherapy. The study period is 24 months, and it is randomly classifi

Eligibility

Sex/Gender

All

Inclusion criteria

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

Design outcomes

Primary

Measure	Time frame
Re-intervention rate	—

Secondary

Measure	Time frame
Procedure related complication, Postoperative complication	—

Countries

Korea, Republic of

Contacts

Public ContactSeung Min Bang

Yonsei University Health System, Severance Hospital

bang7028@yuhs.ac+82-2-2228-1995

Outcome results