JPRN-jRCTs051190072
Completed
未知
Prospective study regarding the improving effect of Go-sha-jinki-gan on frailty(Single-group, open-label study)
Hagihara Keisuke0 sites20 target enrollmentNovember 7, 2019
ConditionsFrailty or prefrailty.
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Frailty or prefrailty.
- Sponsor
- Hagihara Keisuke
- Enrollment
- 20
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Patients who meet a criterion for frailty or pre\-frailty by J\-CHS.
- •2\) Patients with low muscle strength(hand grip strength: less than 26 kg for men and 18 kg for women) or low physical performance (below normal gait speed 1m/s)
- •3\) Patients who are 65 years old or older at the time of informed consent and do not received certification of needed support or needed long\-term care.
- •4\) Patients who can go to hospital for outpatient.
- •5\) Patients who can take Kampo medicine preparations orally.
- •6\) Patients who obtained written consent for this study.
Exclusion Criteria
- •1\)Patients who took Kampo medicine preparation within 4 weeks from the start of treatment.
- •2\)Patients who have allergic episode with Kampo medicine preparations in the past.
- •3\)Patients with obvious joint deformities due to rheumatoid arthritis etc.
- •4\)Patients who has serious complicated disease (disease such as liver, kidney, heart, lung, blood, metabolic, or malignant tumor).
- •5\)Patients who have embedded medical devices such as cardiac pacemakers.
- •6\)Patients suspected of having dementia (MMSE score 23 or below).
- •7\)Patients who are participating in or are planning to participate in clinical trials or other clinical studies.
- •8\)Patients who are considered ineligible to participate by principal investigator or sub\-investigator.
Outcomes
Primary Outcomes
Not specified
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