Skip to content

Effect of concurrent of curcumin and caffeine on non-alcoholic fatty liver disease

Evaluation the Effect of concurrent of curcumin and caffeine on biochemical markers,oxidative stress, and inflammatory cytokines in individuals with non-alcoholic fatty liver disease (Random Clinical trial Study)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240715062438N1
Enrollment
30
Registered
2024-07-30
Start date
2024-07-22
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Non-alcoholic fatty liver disease. Fatty (change of) liver, not elsewhere classified

Interventions

Intervention 1: Intervention group: Eligible participants who met the inclusion criteria were randomly assigned to receive curcumin (Sina curcumin tablets, 40 mg nanomicelles) plus a 200 mg caffeine t

Sponsors

Yasouj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the study people aged 18 to 60 years no history of alcohol consumption no other liver disorders, malignancies, cardiovascular, respiratory and kidney disorders no history of weight loss or bariatric surgery in recent years no drug use In the last 3 months the absence of endocrine and metabolic disorders

Exclusion criteria

Exclusion criteria: Pregnancy or breastfeeding in women The patient's unwillingness to continue participating in the study Non-compliance with the supplement Participating in a concurrent trial Allergy to supplements

Design outcomes

Primary

MeasureTime frame
Biochemical markers. Timepoint: 8 weeks. Method of measurement: Colorimetric method.;Oxidative stress. Timepoint: 8 weeks. Method of measurement: Colorimetric method.;Inflammatory cytokine. Timepoint: 8 weeks. Method of measurement: ELISA.

Secondary

MeasureTime frame
Creatinine level. Timepoint: 8 weeks. Method of measurement: colorimetric.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Bagheri

Yasouj University of Medical Sciences

behnaalipoor@gmail.com0743337251

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026