Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07532759

Impact of Intraoperative PTCD Catheter Retention Versus Removal on Postoperative Short-term Outcomes After Pancreaticoduodenectomy in Obstructive Jaundice

Pancreaticoduodenectomy (PD) is a complex surgical procedure commonly performed for tumors of the pancreatic head and periampullary region. Many patients present with obstructive jaundice and undergo preoperative percutaneous transhepatic cholangial drainage (PTCD) to relieve biliary obstruction. However, there is currently no consensus on whether the PTCD catheter should be removed or retained during surgery.

This multicenter, prospective randomized controlled trial aims to compare two intraoperative strategies: removal versus retention of the PTCD catheter during PD. Participants will be randomly assigned to either group. The study will evaluate whether these different approaches influence postoperative outcomes, particularly major complications such as bile leak and severe postoperative morbidity within 90 days after surgery.

In addition to complications, the study will assess recovery after surgery, including return of gastrointestinal function, length of hospital stay, and quality of recovery, as well as laboratory indicators of liver function and inflammation.

The results of this study are expected to provide evidence to guide surgical decision-making regarding PTCD management during PD and to improve patient outcomes.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

About this study

This multicenter, prospective, randomized controlled trial is designed to evaluate the impact of intraoperative management of preoperative percutaneous transhepatic cholangial drainage (PTCD) catheters on postoperative outcomes in patients undergoing pancreaticoduodenectomy (PD).

Participants meeting eligibility criteria will be randomly assigned in a 1:1 ratio to either intraoperative PTCD catheter removal or retention using a centralized randomization system with stratification by study center and a concealed block design. The study follows a parallel-group design without crossover.

Perioperative management, including surgical technique, postoperative care, and complication management, will be standardized across participating centers according to predefined protocols to minimize inter-center variability. Outcome assessment will be conducted by independent evaluators blinded to treatment allocation. Data will be collected prospectively using an electronic data capture (EDC) system with built-in validation rules, audit trails, and centralized monitoring to ensure data quality and integrity.

The primary analysis will focus on estimating the effect size and corresponding confidence intervals for the predefined outcomes, rather than formal hypothesis testing, given the exploratory nature of the study. Multicenter effects will be accounted for in the analysis by incorporating study center as a stratification factor or covariate.

Participants will be followed for 90 days after surgery, during which predefined clinical outcomes and safety data will be systematically recorded. The findings of this study are intended to generate high-quality preliminary evidence to inform optimal intraoperative PTCD management strategies and support the design of future confirmatory trials.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 to 85 years
  • Patients with pancreatic head or periampullary tumors scheduled for pancreaticoduodenectomy
  • Presence of obstructive jaundice and completion of preoperative
  • percutaneous transhepatic cholangial drainage (PTCD)
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
  • American Society of Anesthesiologists (ASA) physical status ≤ II
  • Able to understand the study and provide written informed consent

Exclusion criteria

  • Presence of distant metastasis or locally unresectable disease
  • Severe cardiac, renal, or pulmonary dysfunction that contraindicates surgery
  • Uncontrolled infection
  • Pregnancy or breastfeeding
  • History of major surgery within 4 weeks prior to enrollment
  • Poor compliance or inability to complete follow-up

Treatment and study plan

PTCD Catheter Removal

Procedure

The preoperative percutaneous transhepatic cholangial drainage (PTCD) catheter is removed intraoperatively during pancreaticoduodenectomy. Removal is performed after completion of the biliary-enteric anastomosis, followed by closure of the hepatic duct puncture site. No external biliary drainage is maintained postoperatively, and only standard abdominal drainage is used.

PTCD Catheter Retention

Procedure

The preoperative percutaneous transhepatic cholangial drainage (PTCD) catheter is retained intraoperatively during pancreaticoduodenectomy. The catheter is used as a stent to support the biliary-enteric anastomosis and is maintained for postoperative external biliary drainage. Planned removal is performed approximately 4 weeks after surgery following confirmation of biliary patency by clamping trial and cholangiography.

Primary outcomes

  1. Composite rate of major postoperative complications

    Time frame: Up to 90 days

    Incidence of a composite endpoint defined as B/C-grade bile leak according to the International Study Group of Liver Surgery (ISGLS) criteria or Clavien-Dindo grade ≥ III complications occurring after pancreaticoduodenectomy.

Secondary outcomes

  1. B/C-grade bile leak

    Time frame: Up to 90 days

    Incidence of B/C-grade bile leak defined according to ISGLS criteria.

  2. B/C-grade pancreatic fistula

    Time frame: Up to 90 days

    Incidence of clinically relevant postoperative pancreatic fistula (grade B/C) defined by ISGPS criteria.

  3. Postoperative infections

    Time frame: Up to 90 days

    Incidence of postoperative infections, including intra-abdominal infection, biliary infection, pulmonary infection, and wound infection.

  4. Time to gastrointestinal recovery

    Time frame: Up to 30 days

    Time to first flatus and time to first oral intake after surgery.

  5. Length of hospital stay

    Time frame: Perioperative

    Total duration of hospitalization after surgery.

  6. Time to initiation of adjuvant therapy

    Time frame: Up to 90 days

    Time from surgery to initiation of postoperative adjuvant therapy.

  7. 90-day readmission rate

    Time frame: Up to 90 days

    Proportion of patients readmitted within 90 days after surgery.

  8. 90-day mortality

    Time frame: Up to 90 days

    All-cause mortality within 90 days after surgery.

Study contacts

Contact information is provided by the study sponsor or research team.

Xu'an Wang, Doctor

CONTACT

[email protected]

+86-15216680015

Sponsors and collaborators

Lead sponsor

Xu'an Wang

Other

Registry information

Official study title

Impact of Intraoperative PTCD Catheter Retention Versus Removal on Postoperative Short-term Outcomes After Pancreaticoduodenectomy in Obstructive Jaundice: An Exploratory Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Apr 16, 2026
Registry last updated
Jul 15, 2026

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.

Published trials that share one or more normalized conditions with this study.