Clinical Trials Logo

Clinical Trial Summary

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?


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02812407
Study type Interventional
Source Mayo Clinic
Contact
Status Withdrawn
Phase N/A
Start date June 2016
Completion date August 2019

See also
  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