Effect of fermented porcine placental extract on fatigue-related parameters in healthy adults

The effect of fermented porcine placental extract on fatigue-related parameters in healthy adults: A double-blind, randomized, placebo-controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005372

Enrollment

Registered

2020-09-02

Start date

2016-10-10

Completion date

Unknown

Last updated

2020-09-07

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 : Subject takes placebo or test material (320mg of fermented porcine placental extract) once a day for 8 weeks.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Participants who voluntarily agrees to participate and signs in informed consent form 2) Healthy men and women (30~59 years)

Exclusion criteria

Exclusion criteria: 1) Subject who is unable to perform treadmill test 2) Those with a high level of cardiopulmonary endurance (maximum oxygen consumption by age of 1st and 2nd grade of 50%) 3) Subject who had a surgical operation 6 months prior to the first visit 4) Smoker, alcoholic and drug addict 5) Subjects who consumed functional foods or oriental medicine within 1 month prior to the first visit 6) Subject who has or experienced following diseases or who takes medicines related to those diseases: hyperlipidemia, asthma, diabetes, bronchitis, anemia, thyroid disease, cardiovascular disease, kidney disease, liver disease, musculoskeletal disorder and nervous system disease 7) Subject who constantly exercised (moderate or high-intensity) for 3 months prior to the first visit 8) Subjects with hypersensitivity to test materials 9) Subject who participated in other human studies within 1 month prior to the first visit 10) Pregnant or lactating women 11) Subject unable to use smartphone 12) Any condition that the principal investigator believes the subject is unsuitable for this study

Design outcomes

Primary

Measure	Time frame
exercise performance and Fatigue-related Parameters	—

Secondary

Measure	Time frame
Clinical pathology examination	—

Countries

Korea, Republic of

Contacts

Public ContactDongHyun Yoon

Seoul National University

Outcome results