Condition 1: Nonalcoholic fatty liver disease. Condition 2: Overweight or Obesity. Nonalcoholic fatty liver disease overweight or obesity
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: non-alcohilic fatty liver disease diagnosed by a radiologist and hepatologist using ultrasonography into one of three categories (mild, moderate or severe degree); age 30–60 years old; overwight or obesity (25=BMI90/140 mmHg); any diagnosed malignancy; breast-feeding, pregnancy and or plan for pregnancy in the next 3 months; professional athlete or regular exercise; treatment with statins, antihypertensive and ursodeoxy colic acid, probiotics and multivitamin-mineral and antioxidant supplements during the three months prior to the intervention; surgery for weight loss in the last year and weight loss program for the past three month; different drugs that interact with cardamom, including aspirin, anticoagulants (warfarin, heparin) and antiplatelet (clopidogrel), non-steroidal anti-inflammatory (ibuprofen or naproxen), blood pressure-lowering drugs, CNS depressants (benzodiazepines such as lorazepam or diazepam, barbiturates such as phenobarbital, narcotics such as codeine, some antidepressants and alcohol), anesthetics, antibiotics, anti-cancer agents, anti-cholinergics, anti-fungals, cyproheptadine, diuretics (loop), estrogen, indomethacin, muscarinic agents, pain relievers and prednisolone; taking a multivitamin-mineral and or antioxidants supplement at least twice a week during study; not taking more than 10% of prescription supplements.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum Irisin. Timepoint: Before and after intervention. Method of measurement: Elisa kit.;Serum Sirtuin1. Timepoint: Before and after intervention. Method of measurement: Elisa kit.;Serum Paraxonase-1. Timepoint: Before and after intervention. Method of measurement: Elisa kit. | — |
Secondary
| Measure | Time frame |
|---|---|
| Serum TNF-a, IL-6 and hs-CRP. Timepoint: Before and after intervention. Method of measurement: Elisa Kit.;FBS, FPI. Timepoint: Before and after intervention. Method of measurement: Kit.;SBP, DBP. Timepoint: Before and after intervention. Method of measurement: mmhg by mercury manometer?.;Serum TG, TC, LDL and HDL. Timepoint: Before and after intervention. Method of measurement: Kit. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tehran University of Medical Sciences