IMPACT of AspireSR® for VNS Therapy on Healthcare Resource Utilisation and Clinical Outcomes.
NCT05975931 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 15
Last updated 2024-12-03
Summary
This is a retrospective non-interventional study to describe the HCRU and clinical outcomes before and after AspireSR® device implantation in subjects with drug resistant epilepsy at the Queen Elizabeth Hospital, Birmingham (QEHB).
Conditions
Sponsors & Collaborators
-
OPEN VIE Limited
collaborator UNKNOWN -
LivaNova
lead INDUSTRY
Principal Investigators
-
Barbara Wysota · The Queen Elizabeth Hospital
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-01-20
- Primary Completion
- 2024-01-30
- Completion
- 2024-01-30
Countries
- United Kingdom
Study Locations
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