| Trial ID: | L0666 |
| Source ID: | JPRN-UMIN000006192
|
| Associated Drug: |
Choline
|
| Title: |
|
| Acronym: |
--
|
| Status: |
Not Recruiting
|
| Study Results: |
No Results Available
|
| Results: |
--
|
| Conditions: |
patients with nonalcoholic fatty liver disease
|
| Interventions: |
The subjects received the oral administration ofcholine (260 mg) under fasting conditions over 12 hours, following that 1-h to 4-h samples (plasma) are obtained.
|
| Outcome Measures: |
Comparison of the plasma free choline levels of fasting and 1-h to 4-h samples with the diagnosis obtained by the liver biopsynan
|
| Sponsor/Collaborators: |
Division of Gastroenterology, Yokohama City University Graduate School of Medicine
|
| Gender: |
All
|
| Age: |
20years-oldNot applicable
|
| Phases: |
Phase 2
|
| Enrollment: |
50
|
| Study Type: |
Interventional
|
| Study Designs: |
Single arm Non-randomized
|
| Start Date: |
18/08/2011
|
| Completion Date: |
--
|
| Results First Posted: |
--
|
| Last Update Posted: |
2 April 2019
|
| Locations: |
Japan
|
| URL: |
https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007317
|
