Gastroparesis Clinical Trial
Official title:
Safety and Efficacy of GPOEM in the Treatment of Gastroparesis
The purpose of this study is to assess the clinical efficacy and safety in the treatment of gastroparesis.
After being informed about the data collected, all the patients affected with gastroparesis
undergoing Gastric Per-Oral Endoscopic Myotomy (GPOEM) will be included in the observational
protocol.
Data concerning pre-operative symptoms and results of the imaging studies will be recorded
together with operative time and operative complications.
Patients will undergo periodical clinical consults and gastric emptying scintigraphy to
assess the improvement in the symptoms and gastric motility.
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