Gastro-esophageal Reflux Disease (GERD) Clinical Trial
Official title:
Baseline Impedance Measured on High Resolution Esophageal Impedance Manometry to Discriminate GERD From Non GERD Patients
Does baseline impedance measured during the landmark phase of esophageal High resolution impedance manometry HRIM correlates with direct mucosal impedance measurement and discriminates GERD from non GERD patients?
Patients referred to the Mayo Clinic Rochester for a clinically indicated high resolution impedance manometry (HRIM), 24 hour impedance pH (MII-pH) study, and esophagogastroduodenoscopy (EGD) will be recruited. Gastroesophageal reflux will be defined as a total 24 hour esophageal acid exposure time ≥5% regardless of concomitant Proton Pump inhibitor (PPI) use. A negative 24 hour MII-pH study will be defined as an acid exposure time ≤2% off PPI therapy or ≤1% if on PPI therapy. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT02471989 -
FODMAPs and Refractory GERD
|
N/A | |
Completed |
NCT02623062 -
Compound Sodium Alginate Oral Suspension Sachet Symptomatic Relief Study
|
Phase 3 | |
Terminated |
NCT02619747 -
Compound Sodium Alginate Oral Suspension Sachet 4-hour Esophageal pH Study in GERD Patients
|
Phase 3 |