CP-Renal: Percutaneous Cryoablation of Central Kidney Tumours With Temporary Renal Artery Occlusion

Sponsor
University Hospital, Strasbourg, France (Other)
Overall Status
Recruiting
CT.gov ID
NCT05461027
Collaborator
(none)
16
1
20
0.8

Study Details

Study Description

Brief Summary

Percutaneous cryoablation is an alternative to urological surgery for T1a tumours, whose oncological efficacy decreases for the most central tumours due to a cold sink effect.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    16 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Percutaneous Cryoablation of Central Kidney Tumours With Temporary Renal Artery Occlusion
    Actual Study Start Date :
    May 1, 2022
    Anticipated Primary Completion Date :
    Dec 31, 2023
    Anticipated Study Completion Date :
    Dec 31, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Description of the technique of percutaneous cryoablation of central renal tumours with temporary balloon obliteration of the renal artery [Files analysed retrospectively from January 01, 2018 to December 31, 2021 will be examined]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion criteria:
    • Adult subject (≥18 years)

    • Subject who has undergone cryoablation of a central kidney tumour with temporary occlusion of the renal artery by an endovascular balloon at the HUS during the period 01/01/2018 to 30/12/2021

    • Subject who has not expressed his/her opposition, after information, to the re-use of his/her data for the purpose of this research.

    Exclusion criteria :
    • Subject having expressed his/her opposition to participate in the study

    • Subject under legal protection, guardianship or curatorship

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Service d'Imagerie Interventionnelle - CHU de Strasbourg - France Strasbourg France 67091

    Sponsors and Collaborators

    • University Hospital, Strasbourg, France

    Investigators

    • Principal Investigator: Pierre-Alexis AUTRUSSEAU, MD, Service d'Imagerie Interventionnelle - CHU de Strasbourg - France

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Strasbourg, France
    ClinicalTrials.gov Identifier:
    NCT05461027
    Other Study ID Numbers:
    • 8529
    First Posted:
    Jul 15, 2022
    Last Update Posted:
    Jul 20, 2022
    Last Verified:
    Jul 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University Hospital, Strasbourg, France
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 20, 2022