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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02532790
Other study ID # AiZhang
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date August 2015
Est. completion date July 2020

Study information

Verified date February 2020
Source Nanjing Children's Hospital
Contact Aihua Zhang, M.D.
Phone +8618951769017
Email bszah@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is performed to evaluate the efficacy and safety of various measures in the treatment of HSPN with mild proteinuria in children.


Description:

Henoch-Schonlein purpura nephritis (HSPN) is one of the most common complications of Henoch-Schonlein purpura, and has become one of the main causes of chronic kidney disease in children. However, the diagnosis and treatment of HSPN is still based on the clinical experience, lacking of evidence-based support. This study is performed to explore the biological markers for early prediction of the prognosis and evaluate the efficacy and safety of various measures in the treatment of HSPN in children.

The patients who are proved to get HSPN by renal biopsy will be randomized to receive either prednisone p.o. or angiotensin-converting enzyme inhibitor(ACEI) p.o. We will follow up them for about 2.5 years and compare the efficacy and safety of both measures by monitoring several indexes.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date July 2020
Est. primary completion date July 2020
Accepts healthy volunteers No
Gender All
Age group 2 Years to 16 Years
Eligibility Inclusion Criteria:

- Renal biopsy proved HSPN (ISKDC class II)

- Proteinuria < 25 mg/kg/d

Exclusion Criteria:

- The children with congenital diseases

- Proteinuria=25 mg/kg/d

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Prednisone
1.5mg/kg/d
ACEI
0.2-0.3mg/kg/d

Locations

Country Name City State
China Nanjing Children's Hospital Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Nanjing Children's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disappearance of proteinuria The proteinuria is < 150mg/d 30 months
Secondary Disappearance of hematuria The number of red blood cells is < 3 in each high power field of vision 30 months
Secondary Renal function The glomerular filtration rate is normal 30 months
See also
  Status Clinical Trial Phase
Recruiting NCT02532777 - The Research of Standard Diagnosis and Treatment for HSPN in Children Phase 2