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The Multi-Center Clinical Study of Tang Shen Prescription on Type 2 Diabetic Kidney Disease in Early Stage

The Multi-Center Clinical Study of Tang Shen Prescription on Type 2 Diabetic Kidney Disease in Early Stage

Status
UNKNOWN
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03009864
Enrollment
632
Registered
2017-01-04
Start date
2017-01-31
Completion date
2020-05-31
Last updated
2017-01-04

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

Conditions

Diabetic Kidney Disease

Keywords

Diabetic Kidney Disease, TCM, RCT

Brief summary

This study is a randomized, double-blinded, placebo-controlled clinical trial on type 2 diabetic Kidney Disease in early stage ( microalbuminuria excretion rate = 20-200mg/min) to evaluate the therapeutic effect of tang shen prescription. 632 participants will be recruited for the study, all of whom had type 2 diabetes, serum creatinine concentrations is normal, and no evidence of non-diabetic renal diseases. The subjects will be randomized to treatment with either tang shen prescription or placebo.

Detailed description

This study is a randomized, double-blinded, placebo-controlled clinical trial on type 2 diabetic Kidney Disease in early stage ( microalbuminuria excretion rate = 20-200ug/min) to evaluate the therapeutic effect of tang shen prescription.632 participants will be recruited for the study, all of whom had type 2 diabetes, serum creatinine concentrations is normal, and no evidence of non-diabetic renal diseases. The study will last for 24 weeks. Subjects will be randomly divided into two groups, either tang shen prescription or placebo,and both of them would be performed on a basic treatment which includes diabetes education, diabetic diet, rational control of blood glucose, and losartan at 50 mg daily, study group take tang wang prescription. Measurements of microalbuminuria excretion rate, albumin-to-creatinine ration, glomerular filtration rate (GFR), serum creatinine concentrations will be tested monthly, and quantity of 24h urinary protein per three months.

Interventions

DRUGTangshen Prescription

The prescription contains granules of five Chinese herbal medicines, every bag weighs 4.87g, take it one bag each time, two times a day.

DRUGPlacebos

Treatment with placebo corresponding to each dose of Tangshen Prescription , every bag weighs 4.87g, take it one bag each time, two times a day.

Sponsors

The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine
CollaboratorOTHER
Zhengzhou City Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Shijiazhuang City Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
Baoding City Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
Hubei Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Changchun Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
Xingtai City Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
Medicine Zibo Wanjie Tumor Hospital
CollaboratorUNKNOWN
Zouping Country Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
She Country Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
Beijing Hospital of TCM
CollaboratorUNKNOWN
Baishi Hospital
CollaboratorUNKNOWN
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of type 2 diabetic Kidney Disease in early stage; 2. Aged 30-70; 3. Signed the informed consent.

Exclusion criteria

1. Non-diabetic renal disease, such as gout, essential hypertension, tumors, and chronic kidney disease which may cause proteinuria or microalbuminuria. 2. Cardiovascular disease、hepatopathy、kidney disease and hematopoietic disease et al, the serum transaminase was two times larger than the normal valuet、serum creatinine concentration greater than the upper limit of normal value and psychiatric disease. 3. Women with Pregnancy or prepare for pregnancy or lactating. 4. Degree of renal failure have developed to the stage of hypoxemia and uremia. 5. Patients participate in other clinical researchers within a month. 6. Patients have been treated with the angiotensin receptor blocker (ARB) drugs to treat diabetic kidney disease except for losartan within a month. 7. Patients have been treated with angiotensin-converting enzyme inhibitors (ACEI) drugs to treat diabetic kidney disease within a month. 8. Systolic blood pressure over 160mmHg or diastolic blood pressure over 100mmHg. 9. Patients with diabetic ketosis, ketoacidosis and severe infections within a month. 10. Patients addicting alcohol, psychoactive substances within 5 years. 11. According to the researcher's judgment, there are other diseases or situations that can reduce the possibility of entering the group or complicate the group, such as frequent changes in the working environment and unstable living environment.

Design outcomes

Primary

MeasureTime frame
changes of albumin-to-creatinine ration0 week,4 weeks, 8 weeks,12weeks,16weeks, 20weeks, 24weeks

Secondary

MeasureTime frame
number of participants of diabetic kidney disease in macroalbuminuria stage0 week, 4 weeks,8 weeks, 12weeks,16weeks, 20weeks, 24weeks
number of participants whose microalbuminuria excretion rate < 20ug/min0 week, 4 weeks, 8 weeks,12weeks,16weeks, 20weeks, 24weeks
change of GFR0 week, 4 weeks, 8 weeks,12weeks,16weeks, 20weeks, 24weeks
the rate of doubling the baseline with serum creatinine value0 week, 4 weeks, 8 weeks,12weeks,16weeks, 20weeks, 24weeks

Countries

China

Contacts

Primary ContactFengmei Lian, PHD
lfm565@sohu.com0086-010-88001402

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026