Clinical Trial Details

Trial ID: L0584
Source ID: IRCT2015122425686N1
Associated Drug: Capparis Spinosa Fruit pickle
Title: The investigation of the effects of Capparis Spinosa Fruit pickle (Traditional Iranian Medicine product) on Liver Transaminases in Nonalcoholic Fatty Liver Disease (NFLD)
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Nonalcoholic fatty liver disease. <br>Nonalcoholic fatty liver disease (NAFLD);Nonalcoholic fatty liver disease (NAFLD)
Interventions: Intervention 1: Intervention 1 : the intervention group In addition to teaching life style and training package similar at baseline and follow up with phone calls weekly, daily intake of 40 mg pickled capers fruit with meals for lunch and dinner. Interve
Outcome Measures: SGPT. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.;SGOT. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.Total chlo. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.;FBS. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.;TG. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.;VLDL. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.;LDL. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.;HDL. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.;Fasting Insulin. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.;Cs-CRP. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Blood sample.;BMI. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: Digital weighing scales and measuring the height of meters.;Appetite. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: VAS Questionnaire.;Insulin resistance. Timepoint: Before the intervention, the end of the twelfth week intervention. Method of measurement: HOMA Index.
Sponsor/Collaborators: Vice chancellor for research, Tabriz University of Medical Sciences
Gender: All
Age: 12 years80 years
Phases: Not applicable
Enrollment: 50
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment.
Start Date: 10/05/2016
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/21439