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The efficacy and safety of Ninjin'yoeito for anorexia, apathy in dementia.

Not Applicable
Conditions
Anorexia in dementia with apathy
Dementia/Anorexia/Apathy
Registration Number
JPRN-jRCTs031200079
Lead Sponsor
Arai Tetsuaki
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

1. Alzheimer type dementia, Dementia with Lewy Bodies or Dementia associated with Parkinson's disease
2. MMSE less than 23
3. Neuropsychiatric Inventory subcategory scores for apathy 1 point or above
4. Neuropsychiatric Inventory subquestion scores for a loss of appetite 3 points or above
5. Treatment has been kept for psychotropic, antiulcer, estrogen, ACEI and zinc compound
6. Treatment has been kept for donepezil, galantamine, rivastigmine, memantine, antipsychotic, antiparkinson and steroid.
7. Agreement to sign an informed consent from patient, legal representative, study partner. Have a study partner able to provide an independent evaluation of functioning
8. Location; outpatient, inpatient, has been kept.
9. A patient who is able to take oral medications.
10. A patient who was informed dementia.

Exclusion Criteria

1) Complications that may affect cognitive function.
2) Severe agitation/aggression
3) Major depression or bipolar disorder within the previous a year. Alcoholism within the previous 2 years, history of drug addiction, Vitamin B12 deficiency, folate deficiency, syphilis or thyroid disorders.
4) Digestive disorders
5) Patients with a life-threatening disease such as malignant tumor
6) Use of prohibited medication (prokinetic agent, stomachics and digestives, some kampo) within the previous 4 weeks
7) Participation in other studies within the previous 12 weeks.
8) Allergic to kampo
9) Pseudohyperaldosteronism
10) Potassium value is less than 3.0mEq / L
11) A patient who is not able to take kampo because of dysphagia.
12) Remarkable hypertension, edema
13) Heart failure, Kidney failure, Decompensated cirrhosis
14) A patient who takes glycyrrhizin

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Anorexia at 12 weeks compared to baseline (NPI score)
Secondary Outcome Measures
NameTimeMethod
Total score of NPI<br>Subscale of NPI<br>Food intake<br>Vitality Index<br>MMSE,FAB<br>Weight, Anemia, CONUT, Albumin
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