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The Theory Study of

The Theory Study of

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002846
Enrollment
Unknown
Registered
2012-11-12
Start date
2011-07-27
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Alzheimer's disease

Interventions

Experimental group:Bushenyisui formulas
Control group:Hydrochloride donepezil

Sponsors

The second hospital affiliated toTianjin university of traditional Chinese medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Accord with dementia and alzheimer's disease diagnosis standard (the DSM-IV standard); 2. TCM syndrome diagnostic for kindney-essence insufficient; 3. Aged 60 to 85 years old; 4. HIS <=4 points; 5. HAMD <=7 points; 6. Subjects and/or its guardian informed agreement signed; 7. CDR=1.0.

Exclusion criteria

Exclusion criteria: 1. People with vascular dementia or other causes of dementia caused by one; 2. With severe heart, liver, kidney and hematopoietic system disease (Sinus bradycardia and conduction blockAspertate aminotransferaseCereal third transaminase More than 2 times of the normal cap; Urea nitrogen more than 1.5 times the normal capThe serum creatinine more than normal range); 3. Allergic constitution or Donepezil HClpiperidine derivatives allergies; 4. Nearly a month may influence the use of any history of drug of cognitive function; 5. The drug therapy failed to control high blood pressure (Systolic blood pressure is greater than 180 mmHg or Diastolic pressure is higher than 100 mmHg); 6. be provided with diseases which Interference cognitive tests, such as aphasiahemiplegia and others(Severe hearing, vision defectsthe difficulty of Verbal communication, eg.); 7. A history of syncope, asthma history and history of chronic obstructive pulmonary disease; 8. Taking part in other drugs in clinical subject; 9. Critical illnessHard to study the efficacy and safety of the drug to make exact evaluation.

Design outcomes

Primary

MeasureTime frame
Blood routine test;Urine routine test;stool routine test;glutamic-oxalacetic transaminase;ALT;BUN;adrenocorticotrophic hormone;Plasma cortisol;growth hormone;estradiol;testosterone;catecholamine;acetylcholine;vasoactive intestinal peptide VIP;thyrotropin;Cr;Interleukin - 1;

Secondary

MeasureTime frame
Interleukin - 2;garma interferon;T Lymphocyte subsets;Total Tau protein;Phosphorylated Tau protein;Beta Amyloid protein 1-42;transforming growth factor;

Countries

China

Contacts

Public ContactYulian Zhang
doctorzhangyulian@163.com+86 13821151196

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 4, 2026