GI Neuromuscular Pathology Prospective Registry

Status Recruiting

Clinical Trial Summary

In this research study, biopsy samples will be collected to provide more insight into the underlying cause of the motility disorders, help direct further investigation into the cause of the underlying condition, provide future prognosis and predict response to gastric electrical stimulation (GES).

Clinical Trial Description

Biopsies will be collected from patients that have been diagnosed with gastroparesis (having nausea, retching, bloating and fullness of stomach) and are undergoing surgery for the GES implantation. These patients will serve as our study group population. Biopsy samples of those who do not have gastroparesis but are undergoing surgery on the digestive system will be collected after the patients consent to be on the trial. These patients will serve as our control group population. Detailed medical history will be collected and the study group patients will be asked to complete two questionnaire to assess the severity of the symptoms. They will be followed in the clinic at 6, 12, 18 and 24 months post implantation. ;

Study Design

Related Conditions & MeSH terms

Gastroparesis

Clinical Trial Details

NCT number	NCT02165059
Study type	Observational [Patient Registry]
Source	Indiana University
Contact	Travis Putzke
Phone	317-278-2064
Email	tputzke@iu.edu
Status	Recruiting
Phase
Start date	December 2013
Completion date	December 2025

View Details

See also
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