Skip to content

Effect of green cardamom on improvement of non-alcoholic fatty liver disease

The effects of green cardamom (Elettaria Cardamomum) supplementation along with lifestyle changes on blood glucose index, lipids, inflammation factors, paraxonase-1, sirtuin-1 and irisin in overweight and obese patients with non-alcoholic fatty liver disease (NAFLD)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015121317254N4
Enrollment
80
Registered
2015-12-27
Start date
2016-01-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Nonalcoholic fatty liver disease. Condition 2: Overweight or Obesity. Nonalcoholic fatty liver disease overweight or obesity

Interventions

Intervention 1: Green cardamom supplementation, 3 gram/day, 3 capsules (1gram)/day with food, for 3 months. Intervention 2: Placebo (bread crumbs) supplementation, 3 gram/day, 3 capsules (1gram)/day w
Treatment - Other
Placebo
Green cardamom supplementation, 3 gram/day, 3 capsules (1gram)/day with food, for 3 months
Placebo (bread crumbs) supplementation, 3 gram/day, 3 capsules (1gram)/day with food, for 3 months

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

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

MeasureTime 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

MeasureTime 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

Public ContactGity Sotoudeh

Tehran University of Medical Sciences

gsotoodeh@yahoo.com+98 21 8895 5742

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 5, 2026