| Trial ID: | L0760 |
| Source ID: | IRCT2013121615825N1
|
| Associated Drug: |
Cichorium
|
| Title: |
Effect of the Root Extract of Cichorium Intybus Formula on Reducing Alanine Aminotransferase (ALT) in Non-alcoholic Fatty Liver Disease: A Randomized Double-blind Clinical Trial Including Placebo
|
| Acronym: |
--
|
| Status: |
Not Recruiting
|
| Study Results: |
No Results Available
|
| Results: |
--
|
| Conditions: |
Fatty liver disease. <br>Diseases of liver;k70-k77;Diseases of liver
|
| Interventions: |
Intervention 1: Intervention 1: A capsule containing 500 mg of Cichorium intybus root extract is given to the patients group in the morning before breakfast. Intervention 2: Intervention 2: Two capsules containing corn starch are given to the control grou
|
| Outcome Measures: |
Alanine Aminotransferase. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.Aaspartat Aminotransferase. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Fasting blood sugar. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Total Cholesterol. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Triglycerides. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;High-density lipoprotein. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Low-density lipoprotein. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Platelets. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Albumin. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Glucose tolerance test. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Body Mass Index. Timepoint: Before intervention and two months after intervention. Method of measurement: Scale and Meter.
|
| Sponsor/Collaborators: |
School of Traditional Medicine, Traditional Medicine and Materia Medica Research Center Shahid Behes
|
| Gender: |
All
|
| Age: |
18 years70 years
|
| Phases: |
Not applicable
|
| Enrollment: |
60
|
| Study Type: |
interventional
|
| Study Designs: |
Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
|
| Start Date: |
09/06/2014
|
| Completion Date: |
--
|
| Results First Posted: |
--
|
| Last Update Posted: |
22 February 2018
|
| Locations: |
Iran (Islamic Republic of)
|
| URL: |
http://en.irct.ir/trial/14977
|
