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NCT05975931: IMPACT

IMPACT of AspireSR® for VNS Therapy on Healthcare Resource Utilisation and Clinical Outcomes.

Terminated Last updated 3 December 2024
What this trial tests

trial in Epilepsy in 15 participants. Terminated before completion.

Timeline
20 January 2022
Primary endpoint
30 January 2024
30 January 2024

Quick facts

Lead sponsorLivaNova
StatusTerminated
Study typeOBSERVATIONAL
Enrollment15
Start date20 January 2022
Primary completion30 January 2024
Estimated completion30 January 2024
Sites1 location across United Kingdom

Conditions studied

Sponsor

LivaNova — full company profile →

Who can join

18 and older, any sex, with Epilepsy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Epilepsy

Currently open trials in the same condition.

Other LivaNova trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05975931.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing