Last updated: March 5, 2021
Sponsor: Centre Hospitalier Universitaire Dijon
Overall Status: Active - Not Recruiting
Phase
N/A
Condition
Hemorrhage
Deep Vein Thrombosis
Circulation Disorders
Treatment
N/AClinical Study ID
NCT04787120
LOFFROY BALT 2020-1
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patient presenting with an arterial abdominopelvic bleeding or imminent risk ofbleeding, including visceral, muscular or GI territories, requiring embolization,along with angiographic abnormalities
- Patient for whom the use of SQUIDperi had been decided for an embolization
- Patient or authorized representative dully informed and having no objection to theclinical data collection and medical file access
- Patient > 18 years
Exclusion
Exclusion Criteria:
- Patient with severe live failure
- Patient participating in another interventional study
- Vulnerable patients including pregnant women
- Patient not eligible for treatment with liquid embolic agent
- Patients presenting contra-indications to SQUIDperi as describes in the InformationsFor Use (IFU)
Study Design
Total Participants: 110
Study Start date:
April 01, 2021
Estimated Completion Date:
March 01, 2024
Connect with a study center
Chu Dijon Bourgogne
Dijon, 21000
FranceSite Not Available

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