drugset / Trial / NCT05768334
Efficacy and Tolerability of Lubiprostone in Patients With Nonalcoholic Fatty Liver Disease
RandomizedParallel-groupSingle-blindTreatment
Summary
Objectives To evaluate the efficacy, safety, and tolerability of lubiprostone in patients with nonalcoholic fatty liver disease (NAFLD). This study will include 100 patients with nonalcoholic fatty liver disease (NAFLD) recruited from the specialized NAFLD outpatient's clinic in National Hepatology and Tropical Medicine Research Institute (NHTMRI). Study design: Randomized controlled trial.
Timeline
- Start
- 2020-11-01
- Primary completion
- 2023-02-01
- Completion
- 2023-02-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Lubiprostone | Small molecule | 24 ug | Oral |