ClinicalTrials.Veeva

Menu

The Study to Describe Symptom Control and Impact on Daily Life in Gastroesophageal Reflux Disease (GERD) Patients

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Gastroesophageal Reflux Disease

Study type

Observational

Funder types

Industry

Identifiers

NCT01200550
NIS-GBA-DUM-2010/1

Details and patient eligibility

About

The purpose of this study is to evaluate symptoms control and impact on daily life from patients perspective using specific GERD Impact Scale(GIS) questionnaire. The another objective is to obtain local epidemiological data for Bosnia and Herzegovina regarding GERD treatment in primary care.

Enrollment

1,233 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients previously diagnosed with GERD (disease duration =3 years) or newly diagnosed patients that are currently not treated with proton pump inhibitor, for whom specialist or General Practionaire (GP) have previously decided to initiate or change treatment for GERD; Patients should be treated for GERD according to current practice

Exclusion criteria

  • Females of childbearing potential should not be pregnant or nursing

Trial design

1,233 participants in 1 patient group

1

Trial contacts and locations

23

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems