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Pilot Study to prove the reproducibility of the intestinal environment of PMAS System through the production of Equol after intake of Soy Isoflavone

Pilot Study to prove the reproducibility of the intestinal environment of PMAS(Pharmaceutical Meta-Analytical Screening) System through the production of Equol after intake of Soy Isoflavone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008816
Enrollment
36
Registered
2023-09-22
Start date
2023-05-23
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 : This study was conducted using a single-group design. Participants were instructed to consume Soy Isoflavones in the form of capsules. Each capsule contained 60 mg of isoflavones.

Sponsors

HEM Pharma
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy adults who are 19 years of age or older. 2. Individuals who have willingly and voluntarily agreed to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Individuals who have a hypersensitivity or allergy to soy materials, such as soy isoflavones. 2. Individuals who have been determined by the tester to be unsuitable for participation in the human application test. 3. Individuals who have used systemic antibiotics within one week prior to Visit 1. 4. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
The conformity between equol generators and non-generators was confirmed based on the results obtained from both human application tests and PMAS (Pharmaceutical Meta-Analytical Screening).

Secondary

MeasureTime frame
It can be confirmed through medical examination, physical examination, and adverse reaction evaluation conducted at the time of visit.

Countries

Korea, Republic of

Contacts

Public ContactHyun Jin Ku

boazmedical

kuhj1229@handong.edu+82-54-260-3022

Outcome results

None listed

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