ifesyle modifications and personality types for GERD

Not Applicable

• Conditions: Diseases of the digestive system

• Registration Number: KCT0007730
• Lead Sponsor: Yonsei University Health System, Gangnam Severance Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 October 2022

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

patients over 18 and under 76.
-patients who recieved an endoscopy within 12 weeks from their first visit.
-patients who report heartburn/regurgitatio symptoms at least one time/week for the past one months
-patients with a GERD-Q score of over 8
-patients who understand the study protocol and can participate during the study period
-patients who agree to participate in the study
-child bearing patients who agree to contraceptives during the study period

Exclusion Criteria

-patients who cannot receive an endoscopy
-patients with esophageal strictures, peptic stricutres, esophageal varices, long segment Barrett esophagus, active peptic ulcers, peptic ulcer bleeding, malignancies, eosinophilic esophagitis1
-primary esophageal motility disorders
-patients who received surgery of the upper gastrointestinal tract other than simple closure of ulcer perforations or endoscopic reaction of being tumors.
-patients with allergies to antacids, PPIs, P-CABs
-patients receiving medication for psychological disorders
-malignancies within 3 years
-pregnancy or breastfeeding
-past history of psychological disorders within the past 5 years
-expected for hospital admission or surgery
-determined by the investigator to be inappropriate to participate

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Rate of resolution of GERD symptoms

Secondary Outcome Measures

Name	Time	Method
Absolute resolution of GERD symptoms