drugset / Trial / NCT03425097

Fexofenadine Use in Gastroesophageal Reflux Symptoms

NCT03425097 ↗

Phase 2 Terminated 11 enrolled Stanford University
RandomizedCrossoverDouble-blindTreatment

Summary

The investigators wish to study the effectiveness of Fexofenadine (an over the counter allergy pill) for the treatment of gastroesophageal reflux symptoms in patients who still have symptoms despite being on a proton pump inhibitor. The investigators will do this by giving participants both Fexofenadine (an H1 blocker) for 2 weeks and placebo (sugar pill) for 2 weeks. The participants will not know which drug they are getting at a particular time. This will help the investigators better assess the true effectiveness of Fexofenadine.

Timeline

Start
2018-02-07
Primary completion
2019-01-08
Completion
2019-01-08

Outcome

Outcome not reported

Stopped: “The study was terminated due to insufficient evidence for Fexofenadine efficacy to treat GERD symptoms after the interim analysis.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Fexofenadine Unknown 180 mg —