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A human trial of Agrimonia pilosa extract powder on improvement of Liver function

A 8 weeks, multi-center, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Agrimonia pilosa extract powder on improvement of Liver function

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008689
Enrollment
100
Registered
2023-08-08
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

None listed

Interventions

Dietary Supplement : • Agrimonia pilosa extract powder group: once a day, 1 capsule once, after breakfast(350 mg/day, 75 mg/day for Agrimonia pilosa extract powder) • Placebo group: once a day, 1 caps

Sponsors

Wonkwang University, Gwangju Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adult men and women aged 19 years or older and 75 years or less at the screening test 2) Participants whose blood ALT level within 46~135 U/L 3) A person who, after hearing and fully understanding the detailed explanation of this trial, voluntarily decides to participate and agrees in writing to comply with the precautions

Exclusion criteria

Exclusion criteria: 1) Acute or chronic hepatitis patients or individuals with Hepatitis B or Hepatitis C virus infection 2) Individuals with liver cirrhosis, liver cancer, or signs suggestive of liver cancer. 3) Individuals with a BMI of less than 18.5 kg/m^2 or greater than 35 kg/m^2 at screening 4) Those who have taken liver function improving drugs and health functional foods within 1 month prior to screening 5) Those with a history of clinically significant hypersensitivity to Agrimonia pilosa 6) Pregnant or lactating women 7) Women of childbearing potential who do not accept the practice of adequate contraception 8) Those who participated in other clinical trials within 3 months prior to screening 9) A person who is judged unsuitable for participation in the study by the director of the study due to diagnostic test results and other reasons

Design outcomes

Primary

MeasureTime frame
ALT(Alanine Transaminase)

Secondary

MeasureTime frame
Liver fuction index;Lipid metabolism index;Liver fatty index;Inflammation index

Countries

Korea, Republic of

Contacts

Public ContactJin Hee Won

Wonkwang University, Gwangju Medical Center

yuanlaosh@hanmail.net+82-62-670-6417

Outcome results

None listed

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