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Clinical Trial Summary

Humanitarian Device: Authorized by Federal (U.S.A.) Law for use in treatment of chronic intractable (drug refractory) nausea and vomiting secondary to gastroparesis of diabetic or idiopathic etiology.


Clinical Trial Description

Description The Medtronic Enterra II Model 37800 Neurostimulator is a programmable device designed to deliver therapy through gastric electrical stimulation when connected to a lead system. These components comprise the implantable portion of the Medtronic Enterra II system. The operation of the neurostimulator is supported by a clinician programmer. The neurostimulator (Figure 1) operates on a sealed battery and electronic circuitry to provide controlled electrical pulse stimulation, through the implanted lead system. A wide range of noninvasively programmable parameters and stimulation modes are available. The neurostimulator provides current parameter information, via telemetry, when used with the clinician programmer. System Components - Neurostimulator: Medtronic Enterra II Model 37800 - Controlling Devices: Medtronic Model 8840 Clinician Programmer with Model 8870 Application Card. Model 8527 Printer optional. - Lead: Medtronic Enterra Model 4351 Unipolar Lead ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06215547
Study type Interventional
Source Methodist Health System
Contact
Status Enrolling by invitation
Phase N/A
Start date September 15, 2015
Completion date September 14, 2025

See also
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