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Suprapapillary Metal Stent vs. Routine Transpapillary Drainage in Malignant Hilar Biliary Obstruction (SMART-B Trial) (SMART-B)

2026年6月12日 更新者:Hospital de Clinicas de Porto Alegre

Randomized Clinical Trial of Suprapapillary Drainage With Metal Stent vs. Routine Internal-External Transpapillary Drainage in Patients With Malignant Hilar Biliary Obstruction

Malignant hilar biliary obstruction is a condition in which the bile ducts near the liver become blocked due to cancer. This blockage can lead to jaundice (yellowing of the skin and eyes), itching, infection, and impaired liver function. To relieve the obstruction, doctors commonly perform procedures to drain bile and restore its flow.

There are different techniques available for biliary drainage. One common method is percutaneous transpapillary internal-external drainage, in which a catheter is placed through the liver and across the natural opening of the bile duct into the intestine. Another approach is percutaneous suprapapillary drainage using a self-expanding metal stent, which allows bile to drain without crossing into the intestine and may reduce the risk of contamination and infection.

Currently, there is no clear consensus on which of these two techniques is safer or more effective for patients with malignant proximal biliary obstruction. Some studies suggest that avoiding manipulation of the intestinal opening of the bile duct may reduce complications such as infection, but high-quality comparative evidence is lacking.

The purpose of this study is to compare percutaneous suprapapillary drainage with a self-expanding metal stent versus routine percutaneous transpapillary internal-external drainage in patients with malignant proximal biliary obstruction. The study aims to compare the rate of drainage-related complications between the two techniques, as well as to evaluate treatment success, stent patency, and the need for reintervention. In addition, in patients with potentially resectable disease undergoing preoperative biliary drainage, the study will assess and compare surgical outcomes between the two approaches. The results of this study may help determine the safest and most effective drainage strategy for these patients and improve future clinical decision-making.

研究概览

详细说明

Malignant hilar biliary obstruction is most commonly associated with perihilar cholangiocarcinoma and represents a complex clinical condition characterized by impaired bile flow at or above the hepatic duct confluence. The resulting cholestasis may lead to progressive hepatic dysfunction, increased risk of infectious complications, and reduced tolerance to systemic or surgical therapies. In selected patients, preoperative biliary drainage is performed to optimize liver function and reduce perioperative risk prior to major hepatectomy.

Percutaneous biliary drainage is widely used in this setting due to its ability to selectively decompress specific hepatic segments, particularly in complex hilar strictures. The conventional approach consists of transpapillary internal-external drainage, in which a catheter is advanced across the obstruction and through the papilla into the duodenum. While effective in achieving biliary decompression, this technique may disrupt the function of the sphincter of Oddi and facilitate duodenobiliary reflux, which has been implicated as a potential mechanism for infectious complications.

Percutaneous suprapapillary drainage with placement of a self-expanding metal stent represents an alternative strategy. By avoiding transpapillary manipulation, this approach preserves sphincter function and may reduce bacterial contamination of the biliary tree. Early clinical data suggest a favorable safety profile, particularly regarding infectious outcomes; however, direct comparisons with conventional transpapillary drainage remain limited, and available studies are constrained by methodological limitations.

An additional area of uncertainty relates to patients with potentially resectable disease. In this subgroup, the choice of drainage technique may influence not only peri-procedural outcomes but also subsequent surgical management. Concerns have been raised regarding the potential impact of metallic stents on operative complexity and resectability, although robust data are lacking.

This randomized clinical trial is designed to compare two percutaneous drainage strategies within a standardized institutional framework. Patients with an indication for percutaneous biliary drainage will be allocated to receive either transpapillary internal-external drainage or suprapapillary drainage with a self-expanding metal stent. The study includes both patients with unresectable disease and those with potentially resectable malignancies, allowing for evaluation across different clinical scenarios.

All procedures will be performed by experienced interventional radiologists using uniform technical protocols, and patients will be managed according to institutional standards of care. Follow-up will include clinical, laboratory, and imaging assessment as appropriate to routine practice.

The study is designed to generate comparative evidence regarding the safety and performance of these two techniques. In addition, a prespecified subgroup analysis will focus on patients with potentially resectable cholangiocarcinoma undergoing preoperative biliary drainage, in order to explore the impact of drainage strategy on subsequent surgical outcomes.

研究类型

介入性

注册 (估计的)

84

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Cleber R. P. Kruel, Professor
  • 电话号码:8232 +55(51)3359-8232
  • 邮箱:crkruel@hcpa.edu.br

研究联系人备份

  • 姓名:Gabriel L. da Silva, Attending Physician
  • 电话号码:8232 +55(51)3359-8232
  • 邮箱:gablsilva@hcpa.edu.br

学习地点

    • Rio Grande do Sul
      • Porto Alegre、Rio Grande do Sul、巴西、90035-903
        • Hospital de Clinicas de Porto Alegre
        • 接触:
          • Cleber R. P. Kruel, Professor
          • 电话号码:8232 +55(51)3359-8232
          • 邮箱:crkruel@hcpa.edu.br
        • 接触:
          • Gabriel L. da Silva, Attending Physician
          • 电话号码:8232 +55(51)3359-8232
          • 邮箱:gablsilva@hcpa.edu.br
        • 副研究员:
          • Gabriel L. da Silva, Attending Physician
        • 副研究员:
          • Leandro A. Scaffaro, Attending Physician
        • 副研究员:
          • Mauricio Farenzena, Attending Physician
        • 副研究员:
          • Flavia H. Feier, Professor
        • 副研究员:
          • Pablo D. Rodrigues, Attending Physician
        • 副研究员:
          • Tomaz J. M. Grezzana, Attending Physician
        • 副研究员:
          • Marcio F. Chedid, Attending Physician
        • 副研究员:
          • William F. Silvano, Attending Physician
        • 副研究员:
          • Francisco C. B. Lemanski, General Surgery Resident
        • 首席研究员:
          • Cleber R. P. Kruel, Professor

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Age >18 years.
  2. Malignant proximal biliary obstruction on imaging (magnetic resonance cholangiopancreatography or contrast-enhanced abdominal computed tomography) with histopathological confirmation or high clinical and radiological suspicion.
  3. Total bilirubin > 3 mg/dL.
  4. Patients not candidates for potentially curative surgical resection due to locally advanced disease, metastatic disease, or inadequate clinical condition.
  5. Patients with potentially resectable neoplasms, defined as the possibility of achieving complete resection (R0), who meet at least one of the following criteria:

5.1 Estimated future liver remnant <40%, in whom percutaneous portal vein embolization of the side to be resected will also be indicated after initial drainage.

5.2 Prolonged jaundice with total bilirubin >10 mg/dL for more than 14 days. 5.3 Malnutrition, defined as ≥10% unintentional weight loss or albumin <3 g/dL, presumably attributable to cholestasis.

5.4 Indication for neoadjuvant chemotherapy.

Exclusion Criteria:

  1. Tumor with distal extension to the duodenal papilla, precluding suprapapillary drainage.
  2. Prior biliary drainage procedure, either percutaneous (PTBD) or endoscopic (ERCP).
  3. Acute cholangitis, clinically defined as fever (axillary temperature >38°C) and leukocytosis (white blood cell count >10,000/mm³).
  4. Uncorrectable coagulopathy.
  5. Iodinated contrast allergy not amenable to desensitization.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Transpapillary internal-external drainage
Participants undergo percutaneous transpapillary internal-external biliary drainage with placement of a catheter across the obstruction and through the papilla into the duodenum, according to standard institutional practice.
Percutaneous biliary drainage performed by advancing a catheter across the biliary obstruction and through the papilla into the duodenum, allowing internal and external bile drainage.
其他名称:
  • 干预 1
有源比较器:Suprapapillary Self-Expanding Metal Stent Drainage
Participants undergo percutaneous suprapapillary biliary drainage with placement of a self-expanding metal stent across the obstruction without crossing the papilla.
Percutaneous biliary drainage performed by placing a self-expanding metal stent across the biliary obstruction without crossing the papilla.
其他名称:
  • 干预 2

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Acute cholangitis
大体时间:Within 90 days after intervention
Defined by clinical criteria, including fever (axillary temperature >38°C) and leukocytosis (white blood cell count >10,000/mm³), in the absence of another infectious source on abdominal and chest imaging.
Within 90 days after intervention
Acute cholecystitis
大体时间:Within 90 days after intervention
Defined by radiological evidence of cholecystitis associated with fever (axillary temperature >38°C) and leukocytosis (white blood cell count >10,000/mm³).
Within 90 days after intervention
Acute pancreatitis
大体时间:Within 90 days after intervention
Defined by the presence of at least two of the following criteria: abdominal pain consistent with pancreatitis, elevation of amylase and/or lipase greater than three times the upper limit of normal, or characteristic imaging findings.
Within 90 days after intervention
Bile leak
大体时间:Within 90 days after intervention
Defined as intra-abdominal bile leakage due to biliary perforation or at the hepatic puncture site, confirmed by imaging.
Within 90 days after intervention
Hemorrhage
大体时间:Within 90 days after intervention
Defined as clinical or radiological evidence of bleeding requiring blood transfusion or reintervention.
Within 90 days after intervention

次要结果测量

结果测量
措施说明
大体时间
Therapeutic success
大体时间:Within 30 days after intervention
Defined as a decrease in total bilirubin to <3 mg/dL or a reduction of more than 50% compared to pre-drainage levels
Within 30 days after intervention
Mortality
大体时间:Within 90 days after intervention
All-cause mortality following biliary drainage.
Within 90 days after intervention
Need for reintervention
大体时间:Within 30 days after intervention
Requirement for additional percutaneous or endoscopic procedures
Within 30 days after intervention

其他结果措施

结果测量
措施说明
大体时间
Rate of curative surgery
大体时间:Within 180 days of intervention
Number of patients from group A (patients with potentially resectable neoplasms) who undergo potentially curative surgery
Within 180 days of intervention
90-day postoperative mortality
大体时间:Within 90 days of curative surgery
Surgical mortality in patients from Group A (patients with potentially ressectable neoplasms) who undergo potentially curative surgery
Within 90 days of curative surgery
90-day postoperative morbidity
大体时间:Within 90 days of curative surgery
Surgical morbidity in patients from Group A (patients with potentially ressectable neoplasms) who undergo potentially curative surgery according to Clavien-Dindo classification
Within 90 days of curative surgery
Incidence of postoperative liver failure
大体时间:Within 90 days of curative surgery
Incidence of postoperative liver failure in patients from Group A (patients with potentially ressectable neoplasms) who undergo potentially resectable surgery
Within 90 days of curative surgery
Stent patency duration
大体时间:Within 180 days of intervention
Duration of stent patency in patients from group B (patients not candidates for potentially curative resection)
Within 180 days of intervention

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 学习椅:Cleber R. P. Kruel, Professor、Hospital de Clinicas de Porto Alegre

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月15日

初级完成 (估计的)

2028年12月31日

研究完成 (估计的)

2028年12月31日

研究注册日期

首次提交

2026年4月16日

首先提交符合 QC 标准的

2026年4月23日

首次发布 (实际的)

2026年4月30日

研究记录更新

最后更新发布 (实际的)

2026年6月16日

上次提交的符合 QC 标准的更新

2026年6月12日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

All IPD collected throughout the trial

IPD 共享时间框架

Beginning 2 months and ending 2 years after the publication of results

IPD 共享访问标准

Access to individual participant data (IPD) and supporting documents (including the study protocol and statistical analysis plan) will be granted to researchers who provide a methodologically sound research proposal. Requests must specify the intended use of the data and will be reviewed by the study investigators in accordance with institutional policies.

Data will be shared in a de-identified format to ensure participant confidentiality. Access will be provided upon reasonable request to the corresponding author, subject to approval by the investigators and applicable ethical and legal requirements. Data will be made available through secure data transfer methods.

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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