Clinical Trials Directory

Trials / Completed

CompletedNCT02958046

The Efficacy of Lansoprazole and Domperidone Combination on Intragastric and Intraesophageal Acidity

Phase 4 Study, Assessing the Efficacy of Lansoprazole and Domperidone Combination on Intragastric and Intraesophageal Acidity

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Neutec Ar-Ge San ve Tic A.Ş · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate the efficacy of lansoprazole combination with domperidone on intragastric acidity and intraesophageal acidity, GERD symptoms, impedance kinetics, gastric emptying in patients with gastroesophageal reflux disease (GERD).

Detailed description

Objectives of the trial to assess the efficacy of lansoprazole in combination with domperidone on gastric acidity, intraesophageal acidity, GERD symptoms, impedance kinetics and gastric emptying in patients with GERD. 24 hour pH measurement and gastric emptying test will be done at screening visit and after 7 days of drug treatment. Twelve patients will take one tablet for 7 days.

Conditions

Interventions

TypeNameDescription
DRUGLansoprazole/DomperidoneDUOLANS 30/30 mg SR tablet per oral, one tablet daily

Timeline

Start date
2014-01-01
Primary completion
2015-05-01
Completion
2015-08-01
First posted
2016-11-08
Last updated
2016-11-08

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT02958046. Inclusion in this directory is not an endorsement.