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Clinical investigation of ninjin'yoeito on the recovery phase of inpatients with acute illness.

Clinical investigation of ninjin'yoeito on the recovery phase of inpatients with acute illness. - Effect of ninjin'yoeito on the recovery phase in inpatients with acute illness.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000035979
Enrollment
80
Registered
2019-02-22
Start date
2017-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inpatients with acute illness

Interventions

yoeito Extract Granules, 7.5g per day no medication

Sponsors

Japanese Red Cross Kumamoto Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: geriatric patient who hospitalized for acute illness. the patient who can return for follow-up visit by walking or in a wheelchair after discharge from the hospital. the patient who satisfies one of the following two conditions, 1) the patient who is between the ages of 65 and 74 years with BMI less than 18.5, 75 years old or older with BMI less than 20. 2) the patient aged 65 years old or older whose serum albumin level at hospital admission is 3.5 mg / dl or less.

Exclusion criteria

Exclusion criteria: the patient who was judged to be inadequate by the judgment of the examination medical attendant.

Design outcomes

Primary

MeasureTime frame
4 week and 12 week after administration 1) Incidence of readmission, and mortality 2) Nutritional status: Weight,Body mass index,Serum albumin level 3)muscle strength:grasping power,femur circumference 4)QOL(quality of life):SF-36

Countries

Japan

Contacts

Public ContactMasayuki Kashima

Japanese Red Cross Kumamoto Hospital Department of General Internal Medicine

m-kashima@kumamoto-med.jrc.or.jp096-384-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026