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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02184910
Other study ID # 4-2013-0722
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 2013
Est. completion date December 2023

Study information

Verified date March 2019
Source Yonsei University
Contact Yong Chan Lee, MD, PhD
Phone 82-2-2228-1960
Email leeyc@yuhs.ac
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

It is well-known that atrophic gastritis is a major risk factor for gastric cancer, which leads to variations in the serum levels of gastrin, pepsinogen (PG) I, and PGII. We want to assess the effects of age, sex, and Helicobacter pylori status on pepsinogen (PG) level for atrophic gastritis and whether gastric atrophy based on the PG test would be improved after H. pylori eradication.


Recruitment information / eligibility

Status Recruiting
Enrollment 108
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender Female
Age group 19 Years and older
Eligibility Inclusion Criteria:

1. over 19 years

2. the patients who have gastrointestinal discomfort or get esophagogastroduodenoscopy (EGD) for health check up

3. the patients who got the procedure, endoscopic submucosal resection (ESD) for early gastric cancer

Exclusion Criteria:

1. gastrectomy history

2. advanced gastric cancer (impossible to get the gastrectomy)

3. Helicobacter eradication history

4. the patients who have chronic disease

5. cancer patients except gastric cancer within 6 months

6. who cannot perform this study according to research's decision

7. who have bleeding tendency (ex. taking antiplatelet agent, low platelet count or abnormal coagulation time)

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
pepsinogen and gastrin


Locations

Country Name City State
Korea, Republic of Severance hospital 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 change of pepsinogen level before and after H. pylori eradication to compare the change of the pepsinogen level before and after H. pylori eradication and evaluate the correlation between the pepsinogen level and the atrophic gastritis baseline and 6 months
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