Clinical trial
Randomized Multi-Center, Subject and Evaluator Blinded, Parallel-Group Study to Evaluate the Safety and Effectiveness of the Instylla Hydrogel Embolic System (HES) Compared With Standard of Care Transcatheter Arterial Embolization (TAE) / Transcatheter Arterial Chemoembolization (cTACE) for Vascular Occlusion of Hypervascular Tumors; A Pivotal Study
NCT04523350 is registered in ClinicalTrials.gov with Instylla, Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Randomized Multi-Center, Subject and Evaluator Blinded, Parallel-Group Study to Evaluate the Safety and Effectiveness of the Instylla Hydrogel Embolic System (HES) Compared With Standard of Care Transcatheter Arterial Embolization (TAE) / Transcatheter Arterial Chemoembolization (cTACE) for Vascular Occlusion of Hypervascular Tumors; A Pivotal Study
- Lead sponsor
- Instylla, Inc.
- Phase
- Not applicable
- Overall status
- Completed
- Start date
- March 5, 2021
- Completion date
- November 19, 2024
- Enrollment
- 150 (actual)
- Sites
- 15
Conditions
As the registry lists them; a condition with its own page is linked.
hypervascular tumors