Percutaneous Cryoablation of Central Kidney Tumours With Temporary Renal Artery Occlusion
CP-Renal
1 other identifier
observational
16
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started May 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2022
CompletedFirst Submitted
Initial submission to the registry
July 12, 2022
CompletedFirst Posted
Study publicly available on registry
July 15, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2023
CompletedDecember 27, 2024
December 1, 2024
1.7 years
July 12, 2022
December 24, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (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
Adult subject (≥18 years) 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
You may qualify if:
- 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.
You may not qualify if:
- Subject having expressed his/her opposition to participate in the study
- Subject under legal protection, guardianship or curatorship
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Service d'Imagerie Interventionnelle - CHU de Strasbourg - France
Strasbourg, 67091, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Pierre-Alexis AUTRUSSEAU, MD
Service d'Imagerie Interventionnelle - CHU de Strasbourg - France
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 12, 2022
First Posted
July 15, 2022
Study Start
May 1, 2022
Primary Completion
December 31, 2023
Study Completion
December 31, 2023
Last Updated
December 27, 2024
Record last verified: 2024-12