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NCT06006689CompletedPhase 2

Efficacy and Safety of QiShen YiQi Dripping Pills in the Treatment of Diabetic Kidney Disease (Syndrome of Qi Deficiency With Blood Stasis)

A Randomized, Double-blind, Multi-center, Standardise-loaded, Placebo-parallel Controlled Clinical Trial of Efficacy and Safety of QiShen YiQi Dripping Pills in the Treatment of Diabetic Kidney Disease (Syndrome of Qi Deficiency With Blood Stasis)

Source: ClinicalTrials.gov · Last updated 23 Oct 2026

Brief summary (registry, in English)

This study will evaluate the efficacy and Safety of QiShen YiQi Dripping Pills in the treatment of Diabetic Kidney Disease (syndrome of Qi deficiency with blood stasis)

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
228 (actual)
First submitted
17 Aug 2023
Start date
15 Sept 2023
Primary completion date
16 Apr 2025
Lead sponsor
Tasly Pharmaceutical Group Co., Ltd
NCT number
NCT06006689

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 228
  • From 15 Sept 2023 to the primary completion date, 16 Apr 2025
  • 16 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who need to take antiplatelet drugs, the dose was stable for less than 1 month
  • Participating in other clinical studies and taking investigational drugs from other studies within 3 months prior to screening

Other illness

  • Subjects with type 1 diabetes mellitus or other specific types of diabetes
  • Acute complications of diabetes such as diabetic ketoacidosis and hyperosmolar hyperglycemia occurred in the past 3 months
  • Subjects have been clinically confirmed cases of primary glomerular disease, secondary glomerular disease other than DKD or other systemic diseases
  • The presence of uncontrolled hypertension, systolic blood pressure ≥160mmHg and/or diastolic blood pressure ≥100mmHg or Hypotension with a systolic blood pressure \<90mmHg and/or a diastolic blood pressure \<60mmHg
  • Serious diseases of other systemic systems that may affect the judgment of efficacy and safety
  • A history of alcohol or drug abuse with a combination of mental illness and poor control
  • Allergic to the experimental drug or its ingredients

Lab values

  • HbA1c ≥8.5% or fasting blood glucose \>11 mmol/L
  • ALT or AST\> 2 times the upper limit of normal
  • Serum potassium\> the upper limit of normal
  • Patients with unstable basic treatment for lowering blood glucose and blood lipids within the past 3 months, and patients with unstable basic treatment for lowering blood pressure within the past 1 month (changing the type of drugs, such as changing the β-receptor blockers to calcium ion antagonists, etc.)
  • Take the following medications within the last 2 weeks:a. Other drugs for the treatment of DKD (Finerenone, Keluoxin capsule, Qizhi Yishen capsule, SGLT2i drugs, GLP-1 drugs, etc.), b. Calcium oxybenzenesulfonate for the treatment of diabetic retinopathy, c. Chinese patent medicine, Chinese medicine decoction, formula granule and other Chinese medicine preparations with the same composition or function indications, d. Tripterygium wilfordii related preparations, Huangkui capsule

Other

  • Urinary sediment indicates "active" glomerulogenic hematuria
  • Women who are pregnant or breastfeeding, or who have a need to have children during the trial
  • The investigator deems that the patient is not suitable to participate in the study

Who the study is looking for

  • Man or woman between 18-75 years-old
  • Subjects with type 2 diabetes mellitus
  • Subjects with a clinical diagnosis of diabetic kidney disease
  • eGFR≥ 45 mL/min/1.73 m2
  • UACR ≥ 30 mg/g but ≤ 300 mg/g
  • Conformed to the TCM syndrome differentiation standard of chronic heart failure syndrome of Qi deficiency and blood stasis
  • Received Steady dose of ACEI or ARB therapy for chronic heart failure at least 2 weeks before receiving investigational drug
  • Abide by the experimental protocol and cooperate with the data collection according to the researcher's judgment

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (16)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Xiyuan Hospital of China Academy of Chinese Medical Sciences
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BeijingChinaUnknown status
Dongzhimen Hospital of Beijing University of Chinese Medicine
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BeijingChinaUnknown status
The First Hospital of Hunan University of Chinese Medicine
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ChangshaChinaUnknown status
West China Hospital of Sichuan University
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ChengduChinaUnknown status
The Affiliated TCM Hospital of Guangzhou Medical University
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GuangzhouChinaUnknown status
The Second Affiliated Hospital Zhejiang University School of Medicine
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HangzhouChinaUnknown status
Hangzhou Hospital of Traditional Chinese Medicine
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HangzhouChinaUnknown status
Heilongjiang Academy of Traditional Chinese Medicine (Heilongjiang Provincial Hospital of Traditional Chinese Medicine)
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HarbinChinaUnknown status
Kaifeng Hospital of Traditional Chinese Medicine
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KaifengChinaUnknown status
Luoyang Third People's Hospital
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LuoyangChinaUnknown status
Sanmenxia Central Hospital
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SanmenxiaChinaUnknown status
Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
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ShanghaiChinaUnknown status
Shanghai Sixth People's Hospital
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ShanghaiChinaUnknown status
Hebei Province Hospital of Traditional Chinese Medicine
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ShijiazhuangChinaUnknown status
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
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TianjinChinaUnknown status
Shananxi Province Hospital of Traditional Chinese Medicine
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Xi'anChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.