| Trial ID: | L0543 |
| Source ID: | IRCT2016061228411N1
|
| Associated Drug: |
Cichorium
|
| Title: |
Evaluation of the effects of Cichorium intybus seed on treatment of nonalcoholic fatty liver disease,a randomized double_blind clinical trial
|
| 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: Intervention group: Cichorium intybus seed syrup,8cc bid. Intervention 2: Control group: standardized placebo 8 cc bid.;Treatment - Drugs;Placebo;Intervention group: Cichorium intybus seed syrup,8cc bid;Control group: standardized plac
|
| Outcome Measures: |
ALT. Timepoint: before intervention, 1 and 2 months after intervention. Method of measurement: photometric.;AST. Timepoint: before intervention, 1 and 2 months after intervention. Method of measurement: photometric.;FBS. Timepoint: before intervention, 1 and 2 months after intervention. Method of measurement: Fasting blood glucose concentrations.;Triglisirid. Timepoint: before intervention, 1 and 2 months after intervention. Method of measurement: blood test.;Cholestrol. Timepoint: before intervention, 1 and 2 months after intervention. Method of measurement: blood test.;LDL. Timepoint: before intervention, 1 and 2 months after intervention. Method of measurement: blood test.;HDL. Timepoint: before intervention, 1 and 2 months after intervention. Method of measurement: blood test.;BMI. Timepoint: before intervention, 1 and 2 months after intervention. Method of measurement: weight with kilograms on a scale,height with meters with the use of a rubber meter.;The severity of fatty liver. Timepoint: before intervention, 1 and 2 months after intervention. Method of measurement: ultrasound.nan
|
| Sponsor/Collaborators: |
Research Vice chancellor of Zanjan University of Medical Science
|
| Gender: |
All
|
| Age: |
20 years45 years
|
| Phases: |
Phase 2
|
| Enrollment: |
60
|
| Study Type: |
interventional
|
| Study Designs: |
Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
|
| Start Date: |
31/05/2017
|
| Completion Date: |
--
|
| Results First Posted: |
--
|
| Last Update Posted: |
22 February 2018
|
| Locations: |
Iran (Islamic Republic of)
|
| URL: |
http://en.irct.ir/trial/23063
|
