How Does Pre-operative Biliary Drainage in Pancreatic Adenocarcinoma Affect Surgical Outcomes in Pancreatic Cancer Surgery (PBDSOO)

February 25, 2026 updated by: East Lancashire Hospitals NHS Trust

Pre-operative Biliary Drainage in Pancreatic Adenocarcinoma and Its Effect on Surgical Oncological Outcomes

Pre-operative biliary drainage (PBD) is a procedure used to relieve bile duct obstruction, a common issue in patients with pancreatic cancer. The obstruction occurs when a tumor blocks the bile duct, leading to jaundice and other complications. While PBD can help resolve jaundice and improve liver function, its impact on the overall outcomes of pancreatic cancer surgery is still debated.

Recent research has focused on whether PBD before surgery improves patient outcomes, such as surgical success, recovery time, and long-term survival. Some studies suggest that draining the bile before surgery might reduce complications like infections, liver dysfunction, and jaundice-related risks. On the other hand, other research indicates that PBD could increase the chances of infection, delays in surgery, or complications from the procedure itself, such as bile leakage or inflammation.

This study will look at patients undergoing pancreaticoduodenectomy to remove their head of pancreas pancreatic ductal adenocarcinoma over 8 years, and will compare the tumour characteristics of patients who have had PBD vs those who have not. Data will be gathered from the already available histological characteristics. No treatment would be affected and no tissue would be affected.

This research study will focus on oncological characteristics such as tumour progression and lymphatic spread, with overall patient survival as secondary outcome measures.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

  1. INTRODUCTION 1.1 BACKGROUND Pancreatic cancer is the 10th most common cancer in the UK, responsible for the 5th largest cancer death rate (1). Oncological resection in the form of pancreatico-duodenectomy (PD) is the only curative treatment for pancreatic ductal adenocarcinoma (PDAC) affecting the head of pancreas (2). Significant prognostic factors for resected PDAC include R status, tumour size and differentiation, lymph node involvement, the presence of lymphovascular invasion (LVI) and perineural invasion (PNI).

    While up to 70% of patients with PDAC in the head of pancreas have concurrent obstructive jaundice, there is much debate in recent years regarding the role of pre-operative biliary drainage (PBD) (3). PBD is used to treat the adverse effects of obstructive jaundice such as cholangitis, pro-inflammatory status, renal and cardiac dysfunction, hepatic dysfunction and coagulopathy, as well as a bridge to allow neoadjuvant therapy(3-5). Randomised control trials have shown that patients who routinely undergo PBD prior to PD experience a greater rate of complications(4, 6, 7).

    1.2 Rationale for Current Study While there is an increasing amount of evidence demonstrating that PBD carries with it a risk of post operative complications, there is little evidence in the literature investigating if PBD affects oncological staging and disease progression (4, 6, 7). This retrospective study aims to investigate the effect of PBD on known markers of oncological disease severity, compared against patients who proceeded straight to surgery.

  2. Study Objectives To identify level of correlation between PBD and oncological characteristics. 2.1 Study Outcomes It is expected that this study will provide essential information on the association between biliary drainage and oncological progression.

    Primary Outcome Measures Lymph node Ratio Secondary Outcome Measures Presence of Perineural Invasion Presence of Lymphovascular Invasion Disease Free Survival Overall Survival Pancreatic Fistula Rate Resection Margin Status T Stage N Stage

  3. Study Design and Data Collection Methods This will be a retrospective case note review, using data over an 8 year period 2014-2022. Patient information will be gained from the electronic patient record. Statistical analysis will then be performed after gathering information from the electronic patient record. There will be no change in patient care or patient interaction in this study. Subjects will be patients who underwent pancreaticoduodenectomy at ELHT for PDAC of the head of the pancreas. The number of patients is currently unknown. Data will be collected onsite at ELHT, a tertiary HPB referral centre. Data is stored on a secure hospital database that is password protected. A MESh check will be performed to check if patients have opted out from their data being used for research.

    3.1 Study Outcome Measures Primary Outcome Measures Lymph node Ratio Secondary Outcome Measures Presence of Perineural Invasion Presence of Lymphovascular Invasion Disease Free Survival (days) Overall Survival (days) Pancreatic Fistula Rate (%) Resection Margin Status (R1/0) T Stage (T1-4) N Stage (N0-2) 3.2 Study Setting Data will be collected on East Lancashire Hospitals NHS Trust site on password protected trust computers. Data will be analysed using statistical analysis software such as SPSS or Jamovi.

  4. Sample and Recruitment 4.1 Inclusion criteria

    • Procedure - Pancreaticoduodenectomy
    • Histology - Pancreatic ductal adenocarcinoma at East Lancashire Hospitals NHS Trust
    • Age > 18 years 4.2 Exclusion criteria Patients < 18 years of age Patients who had pancreaticoduodenectomy for benign disease Patients who had pancreaticoduodenectomy with any histology other than pancreatic ductal adenocarcinoma Patients who underwent any other procedure for head of pancreas pancreatic ductal adenocarcinoma Patients who have opted out from being part of research as per the MESH database

4.3 Statistics and Data Analysis Plan This is a retrospective study, therefore sample size calculation in this particular study is not needed as it is only a snapshot study with intent of leading to larger multi-centre study based on the results, however we will aim for 90-100 patients. Patient data will be anonymised and stored on a trust computer.

4.4 Sampling technique

  • This study will look at all patients undergoing pancreaticoduodenectomy at East Lancashire Hospitals NHS Trust between 2014 and 2022, regardless of pre operative tumour stage or lymphatic status, with a minimum of 90-100 patients
  • Patients with PBD will be included regardless of reason behind PBD

4.5 Participant/Sample Recruitment Potential patients will be identified from the Hospital's electronic patient record, and will be carried out directly by the research team are also part of the care team.

All identifiable data will be stored on a secure trust nhs computer and will not be shared with anyone outside of the research team Patients will not be contacted as part of this research as data will be from already stored electronic healthcare records ICD codes will be used to identify patients who underwent surgery (C25, Z90.410, Z90.41, OFBG0ZZ, ODT90ZZ, OFB90ZZ, ODB90ZZ) Informatics will gather a list of patient details we can access Patients will be cross referenced against MESH database and those who have opted out from being part of research will be excluded from the dataset.

4.6 Participant/Sample identification We intend to identify eligible patients by reviewing histology reports and electronic medical records of patients who underwent pancreatoduodenectomy in the period specified. This will be carried out by the research team who are also part of the clinical care team.

4.7 Pre-Registration Evaluation Data will be collected retrospectively at a tertiary referral centre and it is stored securely at East Lancashire Hospital Trust (ELHT) on a password protected trust computer.

4.8 Participant Consent Process No participant consent will be required as this data is already held in clinical records in the hospitals electronic patient record 4.9.1 Participant Withdrawal Criteria Patient care will not be affected, and data is being collected after they have completed their treatment course. Therefore, there is no withdrawal criteria as it is not applicable. If patients have not consented for their data to be used in research (as per the MESH ), it would not be included.

4.9.2 Study Intervention No procedures will be involved in the study, and no visits will be required, therefore this is not applicable.

4.9.3 Assessment and Follow-Up No follow up or assessment will take place therefore this is not applicable.

Study Type

Observational

Enrollment (Estimated)

90

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patients undergoing pancreaticoduodenectomy for pancreatic ductal adenocarcinoma with curative intent

Description

Inclusion Criteria:

  • Procedure - Pancreaticoduodenectomy
  • Histology - Pancreatic ductal adenocarcinoma at East Lancashire Hospitals NHS Trust
  • Age > 18 years

Exclusion Criteria:

Patients < 18 years of age Patients who had pancreaticoduodenectomy for benign disease Patients who had pancreaticoduodenectomy with any histology other than pancreatic ductal adenocarcinoma Patients who underwent any other procedure for head of pancreas pancreatic ductal adenocarcinoma Patients who have opted out from being part of research as per the MESH database

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Preoperative biliary drainage
Patients who undergo pre op biliary drainage before surgery
Procedure: Pre operative biliary drainage
ERCP or PTC
No pre operative biliary drainage
Patients who proceed straight to surgery

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
lymph Node ratio
Time Frame: From the day of resection
From pathology report
From the day of resection

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

East Lancashire Hospitals NHS Trust

Investigators

  • Study Director: Daren Subar, East Lancashire Hospitals NHS Trust

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

March 1, 2026

Primary Completion (Estimated)

April 1, 2026

Study Completion (Estimated)

May 1, 2026

Study Registration Dates

First Submitted

February 25, 2026

First Submitted That Met QC Criteria

February 25, 2026

First Posted (Actual)

March 3, 2026

Study Record Updates

Last Update Posted (Actual)

March 3, 2026

Last Update Submitted That Met QC Criteria

February 25, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DEV114

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Due to lack of informed consent to do this

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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