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Evaluate the efficacy and safety of Perilla frutescens extract on improvement of Cognitive Function

Randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Perilla frutescens extract on improvement of Cognitive Function

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008844
Enrollment
100
Registered
2023-10-06
Start date
2022-05-09
Completion date
Unknown
Last updated
2023-10-16

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 : • Perilla frutescens extract group: Once a day, 2 capsule once for 12 weeks • Placebo group: Once a day, 2 capsule once for 12 weeks

Sponsors

SFCBIO
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Age 55 or older at the screening examination and able to communicate smoothly (2) KMMSE~2 of 25-28 (3) Participants who have fully understand the information provide d about the study voluntarily decided to participate and agree to comply with precautions

Exclusion criteria

Exclusion criteria: (1) subjects are now receiving treatment due to SCID (structured clinical interview of DSM-IV) axis I disorder during the screening period, or have a history of treatment within 3 years (2) body mass index (BMI) 2.0 mg/dl (10) pregnant or lactating women (11) Women of childbearing age who did not use the proper methods of contraception (12) A person who is judged unsuitable for participation in the study by the director of the study due to other reasons, including diagnostic test results.

Design outcomes

Primary

MeasureTime frame
ADAS-cog total score;Korean Mini-Mental Status Examination~2 (K-MMSE~2)

Secondary

MeasureTime frame
Brain-Derived Neurotrophic Factor(BDNF);Amyloid ß

Countries

Korea, Republic of

Contacts

Public ContactJongcheon Joo

Wonkwang University Oriental Medical Hospital, Jeonju

jcjoo2000@hanmail.net+82-63-270-1073

Outcome results

None listed

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