Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseinterventionalRules rewrite
Not a traditional drug phase: MRI for Magnetic Resonance Imaging
This is a monocentric, single blind, treatment, single arm study. It is designed to compare the rates of detection of hepatocellular carcinoma (HCC) by ultrasound (US) used in clinical routine vs.
This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.
Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
What the registry says happens
If you join, the listed intervention(s) are MRI. The registry lists allocation as na. This is a monocentric, single blind, treatment, single arm study.
They plan to enroll about 330 people at Lausanne. Taking part typically means using or being fitted with a device plus check-ins.
Official title (unrewritten)
Prospective Comparison of Diagnostic Performance and Cost-effectiveness of US and Abbreviated MRI for Hepatocellular Carcinoma Screening
Interventions: MRI
Primary outcome (registry wording): To compare the diagnostic performance of US+/- CEUS and AMRI for HCC detection in an at-risk population
Who it is for (from inclusion criteria)
Ages 18 Years to any
All adult patients with chronic liver disease and indication for HCC screening according to the European Association for the Study of the Liver recommendations
Who the registry excludes
History of other malignancy
Prior liver nodule categorized as LI-RAD 4, 5 or M
History of liver transplantation
MRI or MRI contrast agent precaution
Any other condition making the patient unsuitable for the study
Patient's refusal of transmission of relevant medical conditions found on the medical examinations performed during the study
This study will collect blood from patients with cancer to study the level of cells which decrease the immune response (suppressor cells) before and after chemotherapy. Patients 18 years of age and older with cancer may participate.
This study aims to provide long-term follow-up care of patients previously enrolled in a vaccine study that involved poxviral vectors. Vectors are sequences of genetic material that can be used to introduce specific genes into genetic makeup.
Background: \- Noncirrhotic Portal Hypertension (NCPH) is caused by liver diseases that increase pressure in the blood vessels of the liver. It seems to start slowly and not have many warning signs.
The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.
What phase is NCT05828446?
Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
Can PlainTrials tell me if I qualify for NCT05828446?
No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.