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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02154659
Other study ID # 4-2013-0680
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2014
Est. completion date December 7, 2015

Study information

Verified date March 2019
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Gastroesophageal reflux disease is increasing worldwide. The causes of reflux symptoms are not found exactly. especially, the postprandial reflux symptoms are more common than the all day reflux symptoms. One of the causes of reflux symptoms is the relaxation of the lower sphincter of the esophagus. But, the sphincter relaxation also occur in normal people. But, there is a difference in postprandial reflux pattens between the patients and the normal people. So, in this study, we want to compare the difference of reflux pattern between the patients who have postprandial reflux symptoms and normal people though the 24hr pH monitoring.


Recruitment information / eligibility

Status Completed
Enrollment 81
Est. completion date December 7, 2015
Est. primary completion date December 7, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria:

1. over 19 years old, male and female

2. normal people (control group, who has no postprandial reflux symptoms

3. patients who have postprandial reflux symptoms (postprandial reflux symptom means that within the last 6 months, postprandial reflux symptoms more than once a week for more than 1 month)

Exclusion Criteria:

1. patients who have nasoesophageal stricture

2. patients who have bleeding tendency

3. patients who have esophageal varix

4. patients who have cardioverter implantation

5. patients who had surgery for esophagus, stomach or duodenum

6. patients who are taking medications, gastrointestinal motility drugs

Study Design


Intervention

Device:
24hr pH monitoring


Locations

Country Name City State
Korea, Republic of Yonsei university College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary The difference of reflux pattern at postprandial period between the patients who have postprandial reflux symptoms and the normal people Primary Outcome - The difference of reflux pattern at postprandial period between the patients who have postprandial reflux symptoms and the normal people The postprandial reflux symptom means that the symptoms more than once for a week for more than 1 month Within the 24 hours after the 24hr pH monitoring
Secondary The difference of esophageal reflux pH between the patients who have postprandial reflux symptoms and the normal people Within the 24 hours after the 24hr pH monitoring
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