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NCT03172520

Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial Nerve Monitoring During Parotidectomy

Terminated NA Results posted Last updated 18 January 2020
What this trial tests

NA trial testing APS electrode in Parotid Gland Disorders in 10 participants. Terminated before completion.

Timeline
1 January 2017
Primary endpoint
30 June 2017
30 December 2017

Quick facts

Lead sponsorMayo Clinic
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment10
Start date1 January 2017
Primary completion30 June 2017
Estimated completion30 December 2017
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Mayo Clinic

Who can join

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

Sponsor's own description

The purpose of this study is to document the safety of the Medtronic automatic periodic stimulating (APS) Electrode Stimulator during a parotidectomy and potentially prevent post-operative facial nerve weakness, which is a relatively common outcome after parotid surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Mayo Clinic trials

Trials by the same sponsor.

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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/NCT03172520.

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