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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04226079
Other study ID # 1911-086-107
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2020
Est. completion date July 2020

Study information

Verified date January 2020
Source Seoul National University Hospital
Contact JIN JU CHOI, M.D.
Phone 01028087284
Email wallet87@hanmail.net
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Cross sectional case-control study investigating the difference of volatile organic compound in the exhaled breath of the patients with GI bleeding and normal population.


Description:

This study investigates the difference of volatile organic compound in the exhaled breath of the patients with GI bleeding and normal population. We aimed to find out the biomarkers for GI bleeding.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date July 2020
Est. primary completion date April 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Adults aged between 20 and 80

- Low possibility of gastrointestinal bleeding was proven by esophagogastroduodenoscopy and colonoscopy which were performed within 1 year.

- NSAID non-user (within 1 months before the date of inclusion)

Exclusion Criteria:

- Diagnosis of malignancy diagnosed within 5 years

- Past medical history of chronic liver disease, chronic kidney disease, chronic lung disease, chronic bronchial disease, asthma

- Surgical history of any kind of gastrectomy

- Surgical history of any kind of lung resection which could impact the patient's lung function.

Study Design


Intervention

Diagnostic Test:
Collection of exhaled breath
Collection of exhaled breath will be analyzed for specific volatile organic compounds which show different distribution between groups

Locations

Country Name City State
Korea, Republic of Jin Ju Choi Seoul Gyunggi-do

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary VOC Patterns Patterns of volatile organic compounds recognized by sensor array 1 day of 1st emergency room (ER) visit for GI bleeding
Secondary Measurement of VOC Qualitative and quantitative assay of volatile organic compounds by GC-MS 1 day of 1st emergency room (ER) visit for GI bleeding
Secondary Change of VOC patterns Change of the patterns of volatile organic compounds recognized by sensor array after recovery from GI bleeding 2nd visit (about 2weeks apart from 1st visit)
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