ClinicalTrials.gov record NCT06720883

Robotically Assisted Surgery For Perihilar Cholangiocarcinoma: A Prospective Study

Record copied from ClinicalTrials.gov: Oct 10, 2026AI summaries generated: Sep 6, 2026

Robotically Assisted Surgery For Perihilar Cholangiocarcinoma: A Prospective Study

StatusRecruitingThe study is currently enrolling participants. Only the study team can say whether a particular person can join.
Study typeObservationalA study in which researchers do not assign participants to a treatment or other intervention. They observe or measure what happens, which may include study visits, tests, questionnaires or a review of medical records.
Age18 years old and older
SexAll
LocationItaly
AI summaryWhat this study is about, in plain languageShow ▾Hide ▴

AI-written from the registry record, not the study's own wording. May contain errors or omissions. Check the registry text on this page and the original record ↗ before acting on it.

This single-center prospective observational study collects clinical, operative, and pathology data on people with perihilar cholangiocarcinoma who undergo robot-assisted major liver resection with biliary reconstruction. It tracks complications up to 90 days, conversion to open surgery, pathology margin status, and survival up to five years. Results will be compared with a historical institutional cohort.

What it is studying. The study is describing outcomes after robot-assisted major hepatectomy with biliary reconstruction for perihilar cholangiocarcinoma, including morbidity (complications and 90-day mortality), conversion to open surgery, surgical margin status, biliary fistula, liver failure, and disease-specific and overall survival up to five years.

What the researchers hope to learn. To analyze morbidity using Dindo-Clavien classification and the Comprehensive Complication Index (including 90-day mortality); measure conversion rate and margin status (R0 vs R1); record biliary fistula and liver failure rates; and estimate disease-specific and overall survival at 1, 3, and 5 years, with comparison to a historical institutional cohort.

What this study is about

The study's own summary, as published on ClinicalTrials.gov. Underlined terms have a short explanation.

Cholangiocarcinoma (CCA) represents the most common biliary tract malignancy, and the second most common primary hepatic malignancy, accounting for 15% to 20% of primary liver tumours. Perihilar cholangiocarcinoma (pCCA) involves the biliary confluence with or without involvement of the right and left hepatic ducts. Complete resection with negative histologic margins is the only chance of cure and the most robust predictor of long-term survival for patients affected by any type of locally advanced CCA. However, the proximity of perihilar tumors to vital structures makes curative excision technically difficult. Minimally invasive approaches are progressively spreading in liver surgery units worldwide. Significant advantages of minimally invasive liver resections, if compared to open one, have been diffusely shown, such as shorter hospital stay and possibility of complex reconstructive procedures similar to those performed in open surgery. Robot-assisted liver surgery represents a natural consequence of such a minimally invasive evolution. This is a monocentric, single arm, observational, prospective study that aims at analyzing the outcomes of robotic major liver resection and biliary recontruction for perihilar cholangiocarcinoma. Among study outcomes, the primary outcome is evaluation of morbidity; secondary outcomes includes conversion rate, margin status, biliary fistula, liver failure, disease specific survival, overall Survival Data related to patient condition (laboratory tests, etc.), surgery performed, and post-surgical course will be collected. The protocol for this study has been developed in accordance with the European Union Good Clinical Practice guidelines and the Declaration of Helsinki, and it has been approved by the Territorial Ethics Committee of the East-Central Veneto Area (CETAEV).

Interventions being studied

Being studied in this trial does not mean the treatment or procedure is approved or available for this condition.

Procedure
  • Major hepatectomy

Eligibility

The criteria exactly as listed on ClinicalTrials.gov. Only the study team can say whether they apply to you.

Inclusion criteria

  • Age≥18 years
  • Histologically proven pCCA or highly presumed bile duct malignancy with difficulties to obtain histological evidence with negative Immunoglobulin G4 (IgG4 sample)
  • Preoperative staging work up performed by abdomen enhanced CT scan.
  • The subject understands the nature of this trial and is willing to comply.
  • Ability to provide written informed consent.
  • Patients treated with curative intent in accordance to international guidelines

Exclusion criteria

  • Distant metastases: peritoneal carcinomatosis, liver metastases, distant lymph node metastases, involvement of other organs.
  • Previous radiotherapy
  • Vascular encasement
  • Patients with high operative risk as defined by the American Society of Anesthesiologists (ASA) score>4.
  • Synchronous malignancy in other organs.
  • Palliative surgery

Study description and what participation involves

The study's detailed description, as published on ClinicalTrials.gov.

Show the detailed description from the registry

Cholangiocarcinoma (CCA) represents the most common biliary tract malignancy, and the second most common primary hepatic malignancy, accounting for 15% to 20% of primary liver tumours. The incidence of bile duct cancers is increasing worldwide, currently accounting for 3% of all gastrointestinal cancers (1). According to the anatomical location it is classified as follows: intrahepatic (iCCA), perihilar (pCCA) and distal (dCCA) subtypes. Approximately 50% of CCA are perihilar, 40% are extrahepatic and only 10% or less are intrahepatic (2). Each type of cholangiocarcinoma is characterised by differences in the tumour biology and management, each has a separate American Joint Committee on Cancer (AJCC) staging system (2). Perihilar cholangiocarcinoma (pCCA), also called Klatskin tumour, involves the biliary confluence with or without involvement of the right and left hepatic ducts (3, 4, 5). It is a challenging disease to manage in the preoperatory setting and during surgery. Painless jaundice is the main symptom at presentation. It often arises rapidly and it is present in 90% of pCCA. Fatigue, anorexia, weight loss and non-specific abdominal pain are other common symptoms. Complete resection with negative histologic margins is the only chance of cure and the most robust predictor of long-term survival for patients affected by any type of locally advanced CCA. However, the proximity of perihilar tumors to vital structures, such as the hepatic artery, portal vein, and hepatic parenchyma, makes curative excision technically difficult. Median survival for patients who cannot undergo surgery is 12 months. Patients who receive radical surgical resection have a 5-year survival up to 40% (6, 7). Radical surgical resection of pCCA usually requires a hemi-hepatectomy, often extended. For this reason, the preoperative assessment of the future liver remnant volume (FLR) is a critical step in the surgical plan. Traditionally, a "safe" liver resection requires a FLR of at least 25% in a perfectly healthy liver. When the organ is compromised by steatosis, chronic cholestasis, cirrhosis or chemotherapy this rate has to increase up to 40% (8, 9). Regional lymphnode metastases are not considered an absolute contraindication to resection, although N+ disease is an independent prognostic factor for worse outcome. Nevertheless, complete lymphadenectomy of the hepatoduodenal ligament is considered an essential step of the surgical procedure. Liver and bile duct resection for pCCA are technically complex procedures: the specimen resection with negative margins requires careful dissection of major vascular structures such as portal vein and hepatic arteries. Once completed the resection the biliary tract must be reconstructed, usually with a Jejunal loop. This step of the procedure is particularly complex and requires high levels of skills and detail, thus, so far, has widely limited the use of laparoscopic surgery to complete the surgical procedure. As previously in other fields of surgery, minimally invasive approaches are progressively spreading in liver surgery units worldwide. Significant advantages of minimally invasive liver resections, if compared to open one, have been diffusely shown. In particular, lower morbidity and shorter hospital stays have been demonstrated in many numerically relevant series. Interestingly enough, greater advantages compared to open surgery have been shown in cases of "laparoscopically difficult" liver resections as right or left hepatectomy. Robot-assisted liver surgery represents a natural consequence of such a minimally invasive evolution. Potential advantages of Robot assisted approach are "intuitive". In particular, in liver surgery the relationship between instrument angle of incidence and plans of action occurs in spatially complex and extremely variable scenarios. More than in other surgical settings, such an articulated spatial interaction needs flexible and harmonic movements warranted in robot assisted interventions. Recent evidence confirms Robot assisted hepatectomies are associated with less postoperative pain and shorter hospital stay if compared to open liver resections. At the same time, both minor and major Robot assisted hepatectomies showed similar oncologic performance, morbidity and mortality profile than open liver resections (10, 11). The key advantage of robotic assistance is to allow complex reconstructive procedures similar to those performed in open surgery (12). The relevant developments already achieved in the field of pancreatic surgery (13) are paradigmatic with relevant future perspectives. Indeed, the Whipple reconstruction phase is now performed in many leading robotic assisted HPB centres. It is easy to predict that in hepatobiliary surgery as well the next steps of development will include major vasculo-biliary reconstructions. AIM OF THE STUDY The aim of the study is investigating the potential advantage of Robotic major liver surgery with biliary reconstruction for pCCA utilising a robotic platform, such as the DaVinci® robotic platform, currently available at the Padova teaching hospital and in use for the HPB service. OUTCOMES Primary Outcomes Morbidity: Defined as major and minor complication rate according to Dindo-Clavien classification (14) and Comprehensive Complication Index (CCI), including ninety-days mortality Secondary Outcomes

  • Conversion rate
  • Margin status (R0 Vs R1)
  • Biliary Fistula: As defined by International Study Group of Liver Surgery (15)
  • Liver failure: As defined by International Study Group of Liver Surgery (16)
  • Disease specific survival
  • Overall Survival (1-3-5 years)

STUDY POPULATION AND METHODS This is a prospective observational study. All patients affected by pCCA that will undergo curative intent surgery that requires biliary reconstruction will be enrolled in the study after the work up for surgery. Preoperative, intraoperative and postoperative data will be collected. The DaVinci® robotic platform available at the Padova University hospital will be utilised primarily. In case of future acquisition of newer or different robotic platforms, those will be utilised as well for the study. The postoperative outcome, morbidity, mortality, pathologic margins, number of lymph nodes collected, and long-term oncologic outcome will be reviewed and compared with the historical cohort of the HPB service of Padova University that includes more than 150 cases completed after 2004. INCLUSION CRITERIA Age≥18 years Histologically proven pCCA Highly presumed bile duct malignancy with difficulties to obtain histological evidence with negative Immunoglobulin G4 (IgG4 sample) Preoperative staging work up performed by abdomen enhanced CT scan. The subject understands the nature of this trial and is willing to comply. Ability to provide written informed consent. Patients treated with curative intent in accordance to international guidelines EXCLUSION CRITERIA Distant metastases: peritoneal carcinomatosis, liver metastases, distant lymph node metastases, involvement of other organs. Previous radiotherapy Vascular encasement Patients with high operative risk as defined by the American Society of Anesthesiologists (ASA) score>4. Synchronous malignancy in other organs. Palliative surgery Pathologic Evaluation All surgical specimens will be submitted for histopathological evaluation by adopting a standardised protocol where only dedicated pathologists with expertise in gastro-intestinal pathology will assess the specimens. To adequately determine residual disease status, five resection planes (common bile duct, proximal bile duct, hepatic artery, portal vein, and liver parenchyma) and one periductal dissection plane will be obtained from each surgical specimen. Histological reports will include the following clinicopathological parameters: tumor's size and differentiation grade, vascular, perineural and intraductal invasion, resection/dissection planes status, tumor growth pattern (mass forming, periductal infiltrating, intraductal, and mixed type), lymph node status and coexisting pathology (inflammation, fibrosis, steatosis, sclerosing cholangitis etc.). The annular resection margins (common bile duct, proximal bile duct, hepatic artery, and portal vein) will be recorded as positive or negative, since their slices are generally 1 to 3 mm thick and a "negative" annular plane ensures a margin of > 1 mm. For non-annular planes (periductal and liver parenchyma), margins will be assessed as positive if cancer is up to 1 mm along the dissection plane in the hepatoduodenal ligament or on the liver transection plane. The presence of severe dysplasia or carcinoma in situ at the surgical margin will be classified as a negative margin. The final pathological staging will be generated according to the revised American Joint Committee on Cancer (AJCC)/Union for International Cancer Control (UICC) TNM staging system 8th edition (17). Statistical analysis Values for categorical variables will be expressed as totals and percentages whereas for continuous variables they will be expressed as medians and ranges or interquartile ranges. Statistical analyses will be performed using the Pearson's chi-squared test or Fisher's test for categorical variables such as Liver failure biliary leakage hemorrhage and other complications and the Kruskal-Wallis rank sum test for continuous variables, such as length of hospital stay, intensive care length of stay etc. The length of follow-up will be calculated from the date of surgery to the date of patient death (overall survival-OS) or the latest follow-up. The durations of follow-up and survival will be expressed as medians (interquartile ranges). Survival and recurrence curves will be calculated using the Kaplan-Meier technique and compared with the log-rank test. A p value < 0.05 will be considered to indicate statistical significance, variables with a p value < 0.1 were considered of marginal statistical significance.

AI summaryWhat participation may involve, in plain languageShow ▾Hide ▴

AI-written from the registry record, not the study's own wording. May contain errors or omissions. Check the registry text on this page and the original record ↗ before acting on it.

Participants undergo robotic major hepatectomy (S1 resection) with hilar lymphadenectomy and biliary reconstruction using a robotic platform; conversion to open surgery is possible if needed. The study team will collect preoperative, intraoperative, and postoperative data, submit surgical specimens for detailed pathology, and monitor complications up to 90 days and survival outcomes up to 5 years. Standard clinical visits, imaging, and blood tests as part of surgical care will occur. Written informed consent is required.

How the study is structured. A prospective, single-arm observational cohort at one center. People scheduled for curative-intent robot-assisted major liver resection with biliary reconstruction are followed before, during, and after surgery. The study records clinical, surgical, and pathology information and tracks outcomes for up to five years. The study does not assign treatments; it records outcomes from standard clinical care and compares them with a historical cohort.

Questions you could ask

These questions are suggestions for a conversation with the study team or your own clinician, not advice.

  • The registry lists this study under Cholangiocarcinoma Cancer; Perihilar Cholangiocarcinoma. Does it apply to my diagnosis?
  • This is an observational study, so the study itself gives no treatment. What would taking part involve for me, and would it change my usual care?
  • The listed sites are in Italy. Is any of them reachable for me, and does the study help with travel?
  • Which of the eligibility criteria would need to be checked with tests before I could join?

More on Marfan syndrome

Important dates

Study start
Jun 7, 2024
Primary completion
Jul 7, 2027 (estimated)
Study completion
Jul 7, 2031 (estimated)
Target enrollment
32 participants (estimated)
Last updated on registry
Dec 6, 2024
Data verified
Oct 10, 2026

Sponsor and research team

The lead sponsor funds and oversees the trial. A pharmaceutical or biotech company sponsor typically means the study is testing that company's drug or device; a hospital, university, or government agency usually indicates investigator-initiated or publicly funded research.

Lead sponsor
Azienda Ospedaliera di Padova
Principal investigator
Prof. Umberto Cillo, Prof. Umberto Cillo
Azienda Ospedaliera di Padova

Central study contact

If you're interested in participating, the central contact can answer general questions about the study — including eligibility requirements and how to find a recruiting site near you. Actual eligibility is determined by the site's medical team.

Participating sites (1)

  • Azienda Ospedaliera di PadovaRecruiting

    Padova, 35121 · Italy

    • Umberto Prof. Cillo, MD · +390498211846 · cillo@unipd.it
    • Francesco Enrico D'Amico, MD · +390498211846 · francescoenrico.damico@unipd.it
    • Umberto Cillo, MD
    • Francesco Enrico D'Amico, MD
    • Enrico Gringeri, MD PhD
    • Vitale Alessandro, MD PhD
    • Lanari Jacopo, MD
    • Domenico Bassi, MD
    • Riccardo Boetto, MD PhD
    • Annalisa Dolcet, MD
    • Alessandra Bertacco, MD PhD
    • Alessandro Furlanetto, MD
    • Clarissa De Nardi, MD

Terms used on this page · explanations by MedicalUpdates.ai

single arm
All participants receive the same treatment or follow the same plan. There is no comparison group within the study.
primary outcome
The main result the study is designed to measure and report on. Other results, called secondary outcomes, are also collected.
overall Survival
The length of time from the start of the study or treatment that participants are alive, whatever the cause of death.
CT scan
An X-ray scan that builds detailed cross-section images of the body. 'High-resolution' CT (HRCT) is used to look closely at the lungs.
written informed consent
The process of explaining a study, including its risks and what participation involves, so that a person can decide freely whether to take part. Consent is usually documented in writing, and a participant can choose to leave the study later.
Inclusion Criteria
The conditions a person must meet to be considered for the study, for example a confirmed diagnosis, an age range or a test result.
Exclusion Criteria
The conditions that rule a person out even if they meet the inclusion criteria, for example other illnesses, certain medicines or pregnancy.
contraindication
A reason a particular test or treatment should not be used for a person, for example a metal implant that rules out an MRI scan.
Study Group
One of the groups in a study. Each arm receives a particular intervention, comparator or no intervention, so the groups can be compared.
cohort
A group of people who share a characteristic, such as a diagnosis, and are studied together. 'Prospective' means they are followed forward from enrolment; 'retrospective' means existing records are reviewed.
follow-up
The period after treatment or enrolment during which participants are observed or contacted, for example to record side effects or outcomes.

The study record on this page is reproduced from ClinicalTrials.gov, a database of the U.S. National Library of Medicine, where it was submitted by the study sponsor. MedicalUpdates.ai does not own this content, is not affiliated with or endorsed by ClinicalTrials.gov, NIH, or the U.S. Government, and does not verify the record. Plain-language notes, the glossary and the questions above are added by this site; text in the boxes marked "AI summary" was written by an AI model and may contain errors. Registry records change over time. Check the original record for the current version and discuss eligibility or participation with a qualified healthcare professional.

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