JPRN-UMIN000042240Completed未知
A clinical study of the efficacy and safety of placenta extract in elderly people with low muscle strength and gait speed -Open label trial- - A research of placenta extract in elderly people with low muscle strength and gait speed
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Japan Bio Products Co., Ltd.
- Enrollment
- 27
Study Overview
Brief Summary
Median gait speed was improved from 0.73 m/s to 0.88 m/s (p<0.001). Median grip strength was unchanged from 14.9 kg before to 15.3 kg after ingestion (p=0.539). Among secondary outcomes evaluated in the exploratory analyses, quality of life was improved.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 65years-old to ot applicable (—)
- Sex
- All
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1)Persons with allergic symptoms to the test food and excipients 2) Persons with difficulty walking or with diseases that are known to affect their ability to move (known muscular disease, peripheral vascular disease causing intermittent claudication, central and peripheral nerve disease (e.g. Parkinson's disease, spinal cord disease, motor neuron disease, etc.), severe dementia, severe diabetes). 3) Any person with a history or suspicion of being affected by cachexia 4) Anyone taking a BCAA supplement. 5) Those who continue to take placenta extract 6) Those who have participated in another clinical trial within the past six months 7) A person who is judged by the principal investigator to be unsuitable to participate in the clinical trial.
Investigators
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