Trial Details

Recruiting
Basic Information
Clinical ID c2567
Identifier TCTR20200203001
Trial Title Comparative measurements of Intestinal permeability by using urine Lactulose/Mannitol ratio between patient with Functional bloating or bloating predominant FGIDs, Inflammatory bowel disease (IBD) and healthy volunteer
Trial URL Visit Original Page
Study Information
Study Results

No results available

Conditions Intestinal permeability__Gastrointestinal symptoms Intestinal permeability Urine Lactulose and Mannitol ratio Bloating Crohn disease ;Intestinal permeability Urine Lactulose and Mannitol ratio Bloating Crohn disease
Interventions All participants were overnight fasted and morning urine samples were collected as baseline. After ingestion of 100 ml solution of 5 g lactulose and 2 g mannitol in water, urine samples were serially collected at 2, 4 and 6 hour. ,All participants were overnight fasted and morning urine samples were collected as baseline. After ingestion of 100 ml solution of 5 g lactulose and 2 g mannitol in water, urine samples were serially collected at 2, 4 and 6 hour. ,All participants were overnight fasted and morning urine samples were collected as baseline. After ingestion of 100 ml solution of 5 g lactulose and 2 g mannitol in water, urine samples were serially collected at 2, 4 and 6 hour.;Experimental Biological/Vaccine,Experimental Biological/Vaccine,Experimental Biological/Vaccine;Measurement of percentage excretion of urine lactulose and mannitol in healthy volunteer,Measurement of percentage excretion of urine lactulose and mannitol in functional bloating,Measurement of percentage excretion of urine lactulose and mannitol in small bowel Crohns diseas
Participant Information
Sponsor Siriraj Medical Research Ceter (SiMR)
City -
Country/Region -
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, OLDER_ADULT
Study Design
Study Type Interventional
Phase Not Available
Time Information
Start Date 2025-04-24
Primary Completion Date -
Completion Date 2019-12-31