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OpenTrials
Completed

NCT Number: NCT05045573

Pathological Results of Aggressive Hepatocellular Carcinomas Treated Using SIRT

The aim of our study is to analyze pathological analysis of surgically treated aggressive hepatocellular carcinomas after radio-embolization.

The investigators aim to demonstrate that a higher dose results in better tumor response while respecting safety conditions, that is, no radiologically induced liver disease.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Uhmontpellier

Montpellier, 34295, France

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • aggressive hepatocellular carcinomas with vascular invasion, large tumors or multifocal distribution

Exclusion criteria

  • Other treatment after SIRT (confounding effect)
  • contraindications for surgery

Treatment and study plan

Primary outcomes

  1. Pathological tumor response

    Time frame: 6 months

    Patients are treated with SIRT, then if the tumor response was adequate, surgery was performed.Analysis after surgery. (6 months after SIRT)

Secondary outcomes

  1. Rate of Healthy liver hypertrophia

    Time frame: day 1

    Rate of Healthy liver hypertrophia

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Registry information

Official study title

Pathological Results After Downstaging of Agressive Hepatocellular Carcinoma Using 90Y-SIRT With Personalized Dosimetry

Acronym: PAHCHS

Important dates

Study start
2014
Primary completion
2021
Study completion
2021
First posted
Sep 16, 2021
Registry last updated
Oct 7, 2021

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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