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Completed

NCT Number: NCT04896931

New Prospective Expanded German Registry of Incidental Gallbladder Carcinoma (PERSUASION)- a Permanent Platform Including All Kind of Biliary Tract Cancers (BTC)

Permanent, prospective, multicenter registry including all kind of oncological therapy lines and procedures, clinical outcome, translational research (biobanking) and QoL for all types of biliary tract cancers.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Universitätsklinikum Freiburg, Freiburg im Breisgau, Baden-Wurttemberg, Germany

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About this study

Permanent, prospective, multicenter registry including all kind of oncological therapy lines and procedures, clinical outcome, translational research (biobanking) and QoL for all types of biliary tract cancers. The registry does not define any medical intervention and does not evaluate the efficacy or safety of the treatment decision made by the investigator. Every adverse event whether related to a treatment or not, will neither be documented in the trial´s eCRF nor be reported to the leading investigators of this study.

Objectives: • To establish a registry with a representative BTC-patient population in German-speaking Europe (mainly DACH region) for current and future research. The study registry is not based on a primary endpoint. The data collection includes (among basic patient-/tumor-/treatment- characteristics) the survey of quality of life (EORTC-C30), a so-called patient-reported outcome (PRO) and - if available - the collection of tissue samples for translational accompanying projects.

  • Clinical data:
  • To analyse potential risk factors associated with BTC-cancer addressing clinical and biological predictors of treatment success and survival
  • To determine the course of disease and QoL throughout all applied therapy lines for patients with BTC
  • To measure progression-free, disease-free and overall survival in different BTC sub-groups, mortality and morbidity for perioperative and palliative therapy procedures
  • Recording of the therapy regimens and therapy sequences used across all treatment lines
  • Molecular data (Data- and Biobanking):
  • To establish a sample collection for future molecular/genetic biomarker characterization to enable for e.g. assessment of the frequency of targetable mutations and associated therapy decisions or progression analysis in baseline and follow-up investigations

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Known biliary-tract cancer including intrahepatic-, extrahepatic- and gallbladder carcinomas
  • age ≥18 years
  • signed informed consent form
  • planned for (or recently started - i.e. within the last 21 days)) neoadjuvant, adjuvant or 1st line therapy

Exclusion criteria

  • Patients who are unable to consent because they do not understand the nature, significance and implications of the registry and therefore cannot form a rational intention
  • Patient under 18 years of age
  • Patient's inability to complete QoL questionnaire or answer the questions.
  • Second-line or further palliative therapies if the patient's first-line therapy was not documented within the study.

Treatment and study plan

Primary outcomes

  1. Establishment of BTC population

    Time frame: Through study completion, an average of 2 years

    To establish a representative BTC-patient population in German-speaking Europe in an agile platform study design for future research

Secondary outcomes

  1. analyse potential risk factors associated with BTC-cancer

    Time frame: Through study completion, an average of 2 years

    Correlate medical history with patient outcome, find prevalent medical history associated with BTC chancer

  2. The course of Quality of Life (QoL) throughout the entire course of therapy for patients with BTC

    Time frame: Through study completion, an average of 2 years

    EORTC-QLQC30 according to EORTC scoring manual

  3. PFS

    Time frame: Through study completion, an average of 2 years

    progression-free survival in different BTC subgroups and therapy lines. As for the main objective, there is no formal secondary endpoint in a registry study. Therfore, in this section we will explain the main data to be collected and the main outcome measures.

  4. DFS

    Time frame: Through study completion, an average of 2 years

    disease-free survival in different BTC subgroups and therapy lines. As for the main objective, there is no formal secondary endpoint in a registry study. Therfore, in this section we will explain the main data to be collected and the main outcome measures.

  5. OS

    Time frame: Through study completion, an average of 2 years

    overall survival in different BTC subgroups and therapy lines. As for the main objective, there is no formal secondary endpoint in a registry study. Therfore, in this section we will explain the main data to be collected and the main outcome measures.

  6. mortality

    Time frame: Through study completion, an average of 2 years

    mortality for perioperative and palliative therapy procedures

  7. morbidity

    Time frame: Through study completion, an average of 2 years

    morbidity for perioperative and palliative therapy procedures

  8. establishment of sample collection (tumorblocks and blood)

    Time frame: Through study completion, an average of 2 years

    establish a sample collection for future molecular/genetic biomarker characterization

Sponsors and collaborators

Lead sponsor

Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest

Other

Registry information

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
May 21, 2021
Registry last updated
Jan 7, 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.

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