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Trials / Withdrawn

WithdrawnNCT01637571

Dexilant Treatment in Gastrointestinal Reflux Disease (GERD Related Non Cardiac Chest Pain

The Effect of Dexilant Treatment on Esophageal Hypersensitivity in GERD Related Non Cardiac Chest Pain Patients

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
University of Iowa · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate a new treatment for non-cardiac chest pain (NCCP) related to gastrointestinal reflux disease (GERD), called Dexilant. The investigators would like to test its effectiveness in treating NCCP. The patient will undergo esophageal balloon distention testing (EBDT) before and after taking the new treatment for one month (Dexilant). EBDT evaluates the sensation and mechanical properties of the esophagus. A catheter with a deflated balloon is placed through the mouth and into the esophagus and the balloon is inflated with water. ECG and labs will be done throughout the study as a measurement of safety.

Conditions

Interventions

TypeNameDescription
DRUGDexilant60mg of Dexilant QD for 12 weeks
DRUGDexilant Placebo60mg of Dexilant placebo QD for 12 weeks

Timeline

First posted
2012-07-11
Last updated
2012-07-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01637571. Inclusion in this directory is not an endorsement.

Dexilant Treatment in Gastrointestinal Reflux Disease (GERD Related Non Cardiac Chest Pain (NCT01637571) · Clinical Trials Directory