YiqiJiangzhuoHuoxueTongluo Method to Delay the Occurrence of End-stage Renal Disease in Diabetic Kidney Disease--Study2

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorLiu Hongfang

About this trial

Using the practical randomized controlled trial designed by Zelen, the subjects were randomly divided into the experimental group and the control group. The experimental group was given the traditional Chinese medicine prescription ' Shenzhuo Decoction ' ( composed of Astragalus membranaceus, Salvia miltiorrhiza, Leech, Raw Rhubarb, Epimedium, Motherwort ) + basic treatment ( including nutrition, lifestyle, hypoglycemic, hypotensive, lipid-lowering, control of other risk factors, etc. ), the control group was given basic treatment, a total of 1 year of drug intervention, followed up for 1 year.

Eligibility criteria

Qualifiers

1 In line with the diagnostic criteria of Western medicine type 2 DKD ;

2 18-80 years old, regardless of gender ;

3 30ml / min / 1.73m2 ≤ eGFR < 60ml / min / 1.73m2 ( eGFR was calculated according to CKD-EPI formula ) ;

4 In line with the diagnostic criteria of qi deficiency and collateral stasis syndrome in traditional Chinese medicine ;

Disqualifiers

1 Patients who are currently receiving other traditional Chinese medicines and Chinese patent medicines with DKD therapeutic effects ;

2 combined with other clear renal diseases, such as polycystic kidney disease, glomerulonephritis, renal tumors ;

3 Patients with acute or chronic infection who needed treatment were judged by the researchers not suitable for inclusion in the study ;

4 Patients who participated in any other research drug study and / or received or had received another research drug or intervention treatment ( within one month before signing the informed consent form ) ;

Trial design

Treatments tested in this trial

  • the traditional Chinese medicine prescription ' Shenzhuo Decoction '
  • basic treatment

Treatment groups

228 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Liu Hongfang

Lead sponsor

Dongzhimen Hospital, Beijing

Sponsor institution

Guang'anmen Hospital,China Academy of Chinese Medical Sciencescancel

Collaborator

First Affiliated Hospital, Sun Yat-Sen University

Collaborator

Tianjin Medical University

Collaborator

Affiliated Hospital of Changchun University of Chinese Medicine

Collaborator

EFONG PHARMRCEUTICRL

Collaborator