Trials / Withdrawn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- Withdrawn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
| Type | Name | Description |
|---|---|---|
| DRUG | Dexilant | 60mg of Dexilant QD for 12 weeks |
| DRUG | Dexilant Placebo | 60mg 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.