Deep Brain Stimulation for the Treatment of Obesity
Completed · Not applicable
Conditions studied: Obesity
In brief
The purpose of this clinical study is to investigate the safety and efficacy of deep brain stimulation (DBS) as a treatment option for obesity.
Key facts
- Study ID
- NCT01512134
- Run by
- Ali Rezai, MD
- People needed
- 3
- Starts
- 2012-01-01
- Expected to finish
- 2016-11-01
- Last updated by the study team
- 2017-03-30
Who can join
Age: 22 and older, up to 60. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- At least 24 months post Roux-en-Y gastric bypass surgery without evidence of a sustained improvement in BMI after gastric bypass surgery for at least 6 months.
- Participant is willing to comply with all follow-up evaluations at the specified times
- Participant is able to provide informed consent
- Fluent in English
You may not qualify if…
- Medical contraindications for general anesthesia, craniotomy, or DBS surgery
- Evidence of neurological disorders, e.g., multiple sclerosis, Parkinson's disease and ischemic stroke, or severe brain atrophy or the presence of subdural hygromas or subdural hematomas.
- Severe cardiovascular, pulmonary, renal, liver, hematological disease, severe coagulopathy, acute infectious process
Where it is running
- The Ohio State University Medical Center — Columbus, Ohio, United States
Full record on ClinicalTrials.gov
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