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Randomized crossover controlled trial of treating diabetic kidney disease with Xiaozheng Qufeng formula

Randomized crossover controlled trial and mechanism study of treating diabetic kidney disease with Xiaozheng Qufeng formula

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084297
Enrollment
Unknown
Registered
2024-05-14
Start date
2024-05-21
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Diabetic kidney disease

Interventions

Group A:In the first stage, individules was treated with Xiaozheng Qufeng granule for 4 weeks, and then stop intervention, entering a 4-week cleansing period. After cleaning period, individules was tr
Group B:In the first stage, individules was treated with placebo for 4 weeks, and then stop intervention, entering a 4-week cleansing period. After cleaning period, individules was treated with Xiaozh

Sponsors

Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: ?Female or male, aged 18-70 years old. ?Meet the diagnostic and staging criteria for G2-3aA2 DKD and the diagnostic criteria for Qi deficiency and blood stasis syndrome. ?Those with stable blood pressure below 140/90mmHg and glycated hemoglobin controlled below 7.5%. ?Those who voluntarily participate in this clinical trial and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: ?Individuals with a history of critical illnesses such as malignant hypertension, myocardial infarction, cerebrovascular accidents, and diabetic ketoacidosis within the past six months. ?Patients with congestive heart failure of Class I-IV. ?Accompanied by other primary and secondary kidney diseases (chronic nephritis, kidney disease caused by hypertension, gout, lupus erythematosus, etc.) ?Not suitable for receiving this treatment plan due to conditions such as cancer, pregnancy, and allergy. ?Those who have participated in other clinical trials in the past 3 months.

Design outcomes

Primary

MeasureTime frame
Urinary albumin-to-creatinine ratio;

Secondary

MeasureTime frame
Traditional Chinese Medicine Syndrome Score;

Countries

China

Contacts

Public ContactQiang Fu

Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine

13693332059@163.com+86 84013293

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026