Clinical Trials Directory

Trials / Terminated

TerminatedNCT02022826

Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in Patients With Symptoms of Gastroparesis

Clinical Management With SmartPill Motility Monitoring System and Validation of the SmartPill Five Hour Cutoff in Patients With Symptoms of Gastroparesis

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
167 (actual)
Sponsor
Medtronic - MITG · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This protocol is designed to validate use of the SPM for diagnosis of delayed gastric emptying in patients with symptoms of gastroparesis and assess impact of a SmartPill study on patient management in the gastroparetic populations. Patients with symptoms of gastroparesis will be recruited. Patients will undergo concurrent gastric scintigraphy and SPM testing to determine the presence or absence of delayed gastric emptying based on predetermined diagnostic cutoffs for each technique.

Conditions

Interventions

TypeNameDescription
DEVICESmartPill Monitoring System

Timeline

Start date
2014-01-01
Primary completion
2017-03-01
Completion
2017-03-01
First posted
2013-12-30
Last updated
2017-11-30
Results posted
2017-11-30

Locations

11 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02022826. Inclusion in this directory is not an endorsement.

Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in Patients With Symptoms of Gastroparesis (NCT02022826) · Clinical Trials Directory