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Multi-center clinical study of Baoshen recipe intervening podocyte high glucose memory in the treatment of diabetic nephropathy

Multi-center clinical study of Baoshen recipe intervening podocyte high glucose memory in the treatment of diabetic nephropathy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052271
Enrollment
Unknown
Registered
2021-10-24
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Diabetic nephropathy

Interventions

Experimental group:Basic treatment of western medicine and Baoshenfang granule
Control group:Western medicine basic treatment and comfort granule

Sponsors

Beijing Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnosis of T2DM; 2. Patients who meet the diagnostic criteria of western medicine for diabetic nephropathy stage IV and are combined with diabetic retinopathy, and urine protein =30g/L, glycosylated hemoglobin <8%, serum creatinine <3mg/dl; 3. Patients with deficiency of both qi and yin and blood stasis blocking collaterals; 4. Aged between 18 and 80 years.

Exclusion criteria

Exclusion criteria: 1. Pregnant or planning to become pregnant and lactating patients; 2. Patients with serious primary diseases such as heart, brain, lung, liver and hematopoietic system, allergic constitution; 3. Unable to cooperate, such as mentally ill; 4. There are active infection foci: such as tuberculosis; 5. Patients with renal disease secondary to various tumors and patients with wasting diseases such as tuberculosis; 6. Those who are participating in clinical trials of other drugs or who have participated in other clinical trials within 12 weeks; 7. Glucocorticoids, immunosuppressants, and Tripterygium wilfordii preparations have been used within 12 weeks.

Design outcomes

Primary

MeasureTime frame
Creatinine;Urinary albumin to creatinine ratio;24 hour urine protein;

Secondary

MeasureTime frame
Soluble advanced glycation end product receptor;Advanced glycation end products in urine;Advanced glycation end products in serum;Connective tissue growth factor;Collagen type IV;Podocyte marker protein;Counting of podocytes with positive expression of FSP-1 antibody;Serum total RNA;miR-21;

Countries

China

Contacts

Public ContactWang Yuefen

Beijing Hospital of Traditional Chinese Medicine

85wyf@163.com+86 15901030566

Outcome results

None listed

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