NCT06215547
Medtronic Enterra II Neurostimulator
UNKNOWN
NAAges 18–70InterventionalTreatmentMethodist Health SystemInvestigator-initiated
~500 participants
Updated 2024-11-20 on ClinicalTrials.gov
What's tested:Enterra HDE
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Treating Self Reported Nausea and Vomiting using Enterra II during procedure
Measured over Up to 30 days
Conditions
Where it's being run
1 sites across 1 statesTexas1
Study leadership
- Sachin Kukreja, MD · PRINCIPAL_INVESTIGATOR · Methodist Heath System
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
chronic intractable (drug refractory) nausea and vomiting secondary to gastroparesis of diabetic or idiopathic etiology in patients aged 18 to 70 years.
Exclusion
Organ transplant
Organic obstruction
Pseudo-obstruction
Prior gastric surgery
Scleroderma
Amyloidosis
History of seizures
Peritoneal or unstable dialysis
Chemical dependency
Pregnancy
Primary eating or swallowing disorders
Psychogenic vomiting
Implanted electronic medical devices
Age \< 18 or \> 70 years
What this trial measures
- Treating Self Reported Nausea and Vomiting using Enterra II during procedureUp to 30 days
Using Enterra II system to prevent self reported Nausea and vomiting during a procedure