Fact CheckerSign in

NCT07814586Not yet recruiting

Prognostic Evaluation and Systematic Re-Assessment of Cholangiocarcinoma Therapy

The Re-ACT Study: Prognostic Evaluation and Systematic Re-Assessment of Chol- Angiocarcinoma Therapy

Source: ClinicalTrials.gov · Last updated 11 Sept 2026

Brief summary (registry, in English)

Prospective observational cohort study including patients with a diagnosis of intrahepatic/perihilar cholangiocarcinoma at the central regional multidisciplinary conference, to assess therapy response, patient-reported quality of life, patient-reported symptoms/experiences and biomarkers. For patients diagnosed with localized unresectable disease, the study will document the multidisciplinary re-assessment of therapy response.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
900 (estimated)
First submitted
2 Sept 2026
Start date
Sept 2026
Primary completion date
Sept 2029
Lead sponsor
Karolinska University Hospital
NCT number
NCT07814586

What you commit to

  • Study type: Observational
  • Planned participants: 900
  • From Sept 2026 to the primary completion date, Sept 2029
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • Age \<18 years

Who the study is looking for

  • Clinical diagnosis of intrahepatic- or perihilar cholangiocarcinoma at the regional multidisciplinary team conference
  • For inclusion in the re-assessment arm, a diagnosis of localized, unresectable cholangiocarcinoma at the regional multidisciplinary team conference and clinically evaluated as candidate for tumor-directed medical therapy

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.