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RECRUITING
NCT06241183
PHASE4

Famotidine and Antacids for Treatment of Dyspepsia

Sponsor: Stony Brook University

View on ClinicalTrials.gov

Summary

The aim of this study is to compare intravenous famotidine, an H2 receptor antagonist, and Maalox/ Mylanta, an oral antacid, in treatment of dyspepsia in the emergency department. The goal of this study is to reduce patients' pain based on the verbal numerical pain scale. The anticipated outcome is for pain levels in both groups to decrease. It is expected that antacids will improve symptoms more quickly and to a greater degree within an hour of taking medication based on the results of similar studies.

Official title: Comparing Intravenous Famotidine and Oral Antacids in the Treatment of Dyspepsia in the Emergency Department

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2023-11-09

Completion Date

2025-12

Last Updated

2025-05-01

Healthy Volunteers

No

Interventions

DRUG

Intravenous Famotidine

Patients in this group will receive 20mg IV Famotidine.

DRUG

Oral Maalox/ Mylanta

Patients in this group will receive 30 ml Maalox/ Mylanta.

Locations (1)

Stony Brook University Hospital

Stony Brook, New York, United States