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A Clinical study to Evaluate the Effect of Moshen Digui prescription by ultrasound infiltration in Patients With Idiopathic Membranous Nephropathy (IMN)

The Effect and Safety of Moshen Digui prescription by ultrasound infiltration in the treatment of Idiopathic Membranous Nephropathy (IMN):A randomized, double-blind, placebo-controlled clinical trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015866
Enrollment
Unknown
Registered
2018-04-25
Start date
2018-05-01
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

Idiopathic Membranous Nephropathy

Interventions

Experimental group:Moshen Digui prescription by ultrasound infiltration
control group :placebo by ultrasound infiltration

Sponsors

Beijing Hospital of Traditional Chinese Medicine, Affiliated to the Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Conform to Western medical diagnostic criteria and TCM syndrome differentiation standards; (2) 24-hour urinary protein quantitation <4g/d and normal renal function (continuous monitoring twice or more); (3) No application of ACEI/ARB contraindications: renal artery stenosis, hyperkalemia, solitary kidney, etc.; (4) Aged 18-75 years; (5) Signing informed consent and willingness to complete the treatment.

Exclusion criteria

Exclusion criteria: (1) Hormones, immunosuppressants and/or Tripterygium glycoside tablets have been used in the past six months. (2) Patients with acute renal failure; (3) Infections, hypertension, and other complications have not been effectively controlled; (4) Incorporate severe primary diseases such as heart, brain, liver or hematopoietic system, malignant tumors, and psychotic patients; (5) Allergies or those who are allergic to multiple drugs; (6) Patients with damaged skin at the waist; (7) Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Urine protein concentration in 24 hours;

Secondary

MeasureTime frame
serum albumin;plasma total protein;BUN;SCr;eGFR;

Countries

China

Contacts

Public ContactWenjing Zhao

Department of nephrology, Beijing Hospital of Traditional Chinese Medicine, Affiliated to the Capital Medical University

54498878@qq.com+86 13621162667

Outcome results

None listed

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