Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 12:46 PM
Ignite Modification Date:
2025-12-24 @ 12:46 PM
NCT ID:
NCT02274961
Eligibility Criteria:
Inclusion Criteria:
* Adults between the ages of 19 and 75 inclusive
* Patient with a history of heartburn or acid regurgitation for at least 3 months.
* Those with episodes of heartburn for 2 days or more during the last 7 days prior to baseline
* Patients negative for erosive esophagitis confirmed by esophagogastroduodenoscopy(EGD) performed within 7 days of screening
* Capable of providing written informed consent, willing and able to a comply with all procedures of the study
Exclusion Criteria:
* History of endoscopic erosive esophagitis(EE) at screening EGD.
* Historical evidence of the following disease/conditions : symptom of Irritable bowel syndrome
* More tha 3cm endoscopic Barrett's esophagus or significant dysplastic changes in the esophagus
* Proton Pump Inhibitor(PPI) within 4 weeks prior to the baseline visit
* H2-receptor antagonist, sucralfate, prokinetics, Non Steroidal Antiinflammatory Drugs(NSAIDs) (except low dose aspirin) during the 2 weeks prior to the screening
* Historical evidence of the following disease/conditions during 3 months: Zollinger-Ellison syndrome, the primary esophageal motility disorders achalasia, esophageal stricture, pancreatitis, gastric ulcer, evidence of upper G.I. malignancy, pancreatitis, malabsorption, severe cardiovascular or pulmonary disease, severe liver disease, severe renal disease, cerebral vascular disease,
* Known hypersensitivity to any component of drug
* pregnancy or lactation (F only)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
19 Years
Maximum Age:
75 Years
Study:
NCT02274961
Study Brief:
Protocol Section:
NCT02274961