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Clinical Trials/ITMCTR2200006493
ITMCTR2200006493
Not yet recruiting
未知

A multicenter, prospective, open, cohort study on the efficacy and safety of integrated traditional Chinese and Western medicine in the treatment of chronic kidney disease stage 3-4

the First Affiliated Hospital of Anhui University of Chinese Medicine0 sitesTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
chronic kidney disease stage 3-4
Sponsor
the First Affiliated Hospital of Anhui University of Chinese Medicine
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Sponsor
the First Affiliated Hospital of Anhui University of Chinese Medicine

Eligibility Criteria

Inclusion Criteria

  • ? Age 18 \~ 70 years old, ? meet the diagnostic criteria of CKD stage 3\-4; ? Blood pressure \< 140/90mmhg, blood potassium \< 5\.5mmol/l, hemoglobin \= 80g/l, infection was controlled, and the condition was stable for more than 2 weeks; ? Those who did not use Chinese patent medicine for CKD within 2 weeks before enrollment, or who had used Chinese patent medicine but had a 2\-week washout period; ? Sign informed consent.

Exclusion Criteria

  • ? Pregnant or lactating patients ? unable to cooperate, such as psychotic patients ? complicated with active malignant tumors, infectious diseases, liver cirrhosis decompensation, hematopoietic system and other serious primary diseases; ? There is acute urinary tract obstructive disease, which needs surgical treatment; ? Severe arrhythmia, heart failure, NYHA grade III or above, or myocardial infarction or cerebrovascular events within 3 months before enrollment; ? Using corticosteroids, non steroidal anti\-inflammatory drugs or immunosuppressants; ? Accord with the clinical or pathological diagnosis of diabetes kidney disease; ? Patients are unwilling to participate and refuse to sign informed consent; ? Patients who are participating in other clinical trials

Outcomes

Primary Outcomes

Not specified

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