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Effect of Multi Vitamin and Mineral Supplementation of Liver Enzymes and Sonography in Patient With NAFLD

S

Sulaimany Polytechnic university

Status and phase

Completed
Phase 1

Conditions

Non-Alcoholic Fatty Liver Disease

Treatments

Combination Product: Placebo
Combination Product: Multiviamins and minerals

Study type

Interventional

Funder types

Other

Identifiers

NCT05897606
KTC1211

Details and patient eligibility

About

The study was performed on 160 participants, to ensure the impact of multi vitamin and mineral to reduce NAFLD

Full description

This study was performed on 160 participants, to ensure the impact of multi vitamin and mineral to reduce NAFLD.

Participants were randomly selected to participate in the study. Then divided into the groups (intervention and placebo). Intervention received supplementation for 12 weeks and placebo received same capsule was made for placebo groups.

Enrollment

160 patients

Sex

All

Ages

22 to 78 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participants with NAFLD diagnosed

Exclusion criteria

  • subjects who in the last 6 months received vitamin or mineral supplementation, those with chronic conditions such as diabetes, hypertension, and heart disease, unwillingness to continue the study protocol, lactating women and pregnant women.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

160 participants in 2 patient groups, including a placebo group

effect multivitamin and minerals on NAFLD for 12 weeks
Experimental group
Description:
The intervention group received one capsule of multivitamin and minerals supplements every day, one hour after breakfast, for 12 weeks.
Treatment:
Combination Product: Multiviamins and minerals
Placebo
Placebo Comparator group
Description:
the control group took a placebo prepared with the same shape and size of supplements.
Treatment:
Combination Product: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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