| Trial ID: | L0872 |
| Source ID: | IRCT2015062922977N1
|
| Associated Drug: |
Cinnamon
|
| Title: |
Evaluating Cinnamon Effects on Clinical, Serologic and Sonographic Characteristics of Non-Alcoholic Fatty Liver Disease patients
|
| Acronym: |
--
|
| Status: |
Not Recruiting
|
| Study Results: |
No Results Available
|
| Results: |
--
|
| Conditions: |
Non-Alcoholic Fatty Liver Disease. <br>Fatty (change of) liver, not elsewhere classified;Fatty (change of) liver, not elsewhere classified
|
| Interventions: |
Intervention 1: In the treatment group (Cinnamon group) all patients will receive 750 mg cinnamon capsules twice daily for 12 weeks starting after initial assessments. Intervention 2: In the control group, all patients will receive 750 mg placebo capsule
|
| Outcome Measures: |
Fatty liver score in ultrasound. Timepoint: Before intervention and after three months of intervention. Method of measurement: Ultrasound evaluations of abdomen.;Fasting Blood Sugar (FBS). Timepoint: Before intervention and after three months of intervention. Method of measurement: colorimetric enzymatic method.;HbA1C. Timepoint: Before intervention and after three months of intervention. Method of measurement: measured by affinity chromatographic method.;Triglycerides, Total Cholesterol, Low-density Lipoprotein (LDL), and High-density Lipoprotein (HDL). Timepoint: Before intervention and after three months of intervention. Method of measurement: Colorimetric Enzymatic Method.;Serum ALT and AST Concentration. Timepoint: Before intervention and after three months of intervention. Method of measurement: UV Test.;Weight (kg). Timepoint: Before intervention and after three months of intervention. Method of measurement: Digital scale with minimal clothing and no shoes.;Body Mass Index (BMI). Timepoint: Before intervention and after three months of intervention. Method of measurement: Weight (kilograms) divided by the square of height (meters).;Waist Circumference. Timepoint: Before intervention and after three months of intervention. Method of measurement: non-stretchable tape without any pressure (cm).nan
|
| Sponsor/Collaborators: |
Deputy of Research Development Ahvaz Jundishapur University of Medical Sciences
|
| Gender: |
All
|
| Age: |
18 years65 years
|
| Phases: |
Phase 1/Phase 2
|
| Enrollment: |
120
|
| Study Type: |
interventional
|
| Study Designs: |
Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
|
| Start Date: |
20/07/2015
|
| Completion Date: |
--
|
| Results First Posted: |
--
|
| Last Update Posted: |
22 February 2018
|
| Locations: |
Iran (Islamic Republic of)
|
| URL: |
http://en.irct.ir/trial/19715
|
