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Completed

NCT Number: NCT03164785

Efficacy and Safety of Jinshuibao Capsule on Diabetic Kidney Disease

The purpose of this study is to investigate the therapeutic effect and safety of Jinshuibao Capsule on diabetic kidney disease in T2DM patients.

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Key information

About this study

Diabetic Kidney Disease (DKD) is one of the most important microvascular complications of diabetes and is the leading cause of end-stage renal disease. Intensive glycemic and blood pressure control, combined with renin - angiotensin system blocking therapy (including ACEI and ARB drugs), has to a certain extent, delayed the progression of DKD, but still cannot completely block its development. Cordyceps sinensis is a traditional Chinese medicine and Jinshuibao Capsule is its artificial preparation, with the effect of renoprotection. However, its clinical application in diabetic kidney disease is not well-defined so far. The aim of this study is to investigate the potential use of Jinshuibao Capsule on microalbuminuria in T2DM.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects with written informed consent.
  • Type 2 diabetes according to 1999 WHO criteria.
  • Age: 30-75 years.
  • HbA1c < 11%.
  • Stage III diabetic kidney disease:

5.1 microalbuminuria: 30 mg / g < urinary albumin creatinine ratio (ACR) < 300 mg / g, positive for at least two in three times.

5.2 renal function: eGFR ≧ 30 ml / min / 1.73 ㎡.

  • Stable use of a standard dose of angiotensin II receptor blocker ≧ 3 months.
  • Childbearing-age women with contraceptive measures.

Exclusion criteria

  • Type 1 Diabetes Mellitus.
  • Non-diabetic urinary system diseases (Urinary tract obstruction, bladder emptying disorders, severe benign prostatic hyperplasia, renal vascular disease, post-renal transplantation, active urinary tract infection,etc.)
  • Other serious diseases [severe hypertension ((defined as SBP > 200 mmHg and/or DBP > 110 mmHg, or requiring ≧3 anti-hypertensive drugs simultaneously), cardiovascular and cerebrovascular events within 6 months, autoimmune diseases implicating the urinary system, chronic or acute pancreatitis, malignancy, hepatic abnormalities (transaminase ≧ 3.0 x UNL), severe gastrointestinal diseases, other endocrine diseases affecting the urinary system, etc.]
  • Allergic to Cordyceps sinensis, use of ACEIs, any use of Cordyceps sinensis preparations, systemic glucocorticoid treatment ≧ 7 days within a month, use of nephrotoxic drugs within 3 months, alcohol or psychotropic drug dependence, etc.
  • Presence of acute metabolic disorders (DKA,HHS); history of surgery, severe trauma and other stress conditions.
  • Female patients who are pregnant or breastfeeding. Any medical condition that, in the opinion of the investigator, will interfere with participation in the trial.

Treatment and study plan

Jinshuibao Capsule

Drug

1.98g t.i.d. p.o. for 6 months

Other names: Jinshuibao Jiaonang, Cordyceps sinensis, Artificial Cordyceps sinensis powder

Primary outcomes

  1. Change in urine albumin creatine ratio (ACR).

    Time frame: Baseline and 1,2,3,6 months.

    First morning urine (10-15ml) of the subject is collected with a clean urine collection tube (or vial).

Secondary outcomes

  1. The incidence of ≧30% decline in eGFR from baseline.

    Time frame: half a year

    Monitoring changes in glomerular functions measured in estimated glomerular filtration rate (eGFR) [CKD-EPI creatinine-cystatin equation (2012)].

  2. Change in urine α1-microglobulin.

    Time frame: Baseline and 1,2,3,6 months.

  3. Change in urine β2-microglobulin.

    Time frame: Baseline and 1,2,3,6 months.

  4. Change in urine N-acetyl-β-D-glucosidase.

    Time frame: Baseline and 1,2,3,6 months.

  5. Change in urine neutrophil gelatinase-associated lipocalin.

    Time frame: Baseline and 1,2,3,6 months.

  6. Change in inflammation level.

    Time frame: Baseline and 1,2,3,6 months.

    Change in hs-CRP level.

  7. Change in HbA1c.

    Time frame: Baseline and 1,3,6 months.

  8. Change in blood pressure control.

    Time frame: Baseline and 1,2,3,6 months.

  9. Change in blood lipids.

    Time frame: Baseline and 1,3,6 months.

  10. Life quality evaluation

    Time frame: Baseline and 6 months.

    Change in SF-36 Scale score.

  11. Incidence of Treatment-Emergent Adverse Events

    Time frame: half a year

    Treatment-related adverse events as assessed by deterioration of liver functions with other reasons excluded, self-report of gastrointestinal symptoms associated with drug intake, etc.

Sponsors and collaborators

Lead sponsor

Second Xiangya Hospital of Central South University

Other

Registry information

Official study title

Efficacy and Safety of Jinshuibao Capsule as Add-on Therapy to Angiotensin II Receptor Blockers on Diabetic Kidney Disease in Patients With Type 2 Diabetes Mellitus

Important dates

Study start
2017
Primary completion
2020
Study completion
2022
First posted
May 24, 2017
Registry last updated
Jan 3, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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