Study on the Treatment of Children With Purpura Nephritis With Huaiqihuang Granules

Sponsor
The Children's Hospital of Zhejiang University School of Medicine (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04623866
Collaborator
(none)
10
2
2
9.9
5
0.5

Study Details

Study Description

Brief Summary

About 20% children with allergic purpura develop nephritis syndrome or nephrotic syndrome, 1% to 7% to kidney failure or end-stage renal disease. Children with serious damage to health, significantly reduced quality of life and caused heavy economic burden to the family . As the pathogenesis of HSPN is complex, it is difficult to formulate an exact individualized treatment plan.

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Detailed Description

Children of Purpura nephritis with moderate protenuria(24 hours urinary protein quantitative 0.5 ~ 1.0 1.73 g/m2 and 24 hours urinary protein amount of not more than 1.0 g) in this study was choosed as participatant, plan randomly into the group of 10 cases, treated with huaiqihuang particles and valsartan for 24 weeks to analyze the curative effect and clinical value of single drug therapy for children with purpura nephritis in reducing proteinuria, protecting renal function and promoting rehabilitation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Single Center Randomized Controlled Clinical Study on the Treatment of Children With Purpura Nephritis With Huaiqihuang Granules
Anticipated Study Start Date :
Nov 1, 2020
Anticipated Primary Completion Date :
Aug 1, 2021
Anticipated Study Completion Date :
Aug 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Huaiqihuang Group

Huaiqihuang granules 60g/1.73m2 bid 24 weeks

Drug: Huaiqinhuang
Huaiqihuang granules are composed of Huaier fungus, Fructus lycii and Huangjing. Studies have shown that huaiqihuang treatment can reduce cytokines in children with purpura nephritis interleukins IL - 4, IL - 10 and the tumor necrosis factor alpha (TNF alpha) expression level, prompt huaiqihuang granule treating children allergic purpura nephritis can significantly improve the clinical curative effect, improve the level of cytokines and the patient's immune function, and does not increase the incidence of adverse reactions.
Other Names:
  • Huaiqihuang granules
  • Active Comparator: Valsartan group

    Valsartan granules 80mg/1.73m2 based qd 24 weeks

    Drug: valsartan
    Valsartan granules 80mg/1.73m2 based qd 24 weeks
    Other Names:
  • Valsartan capsule
  • Outcome Measures

    Primary Outcome Measures

    1. change of urinary protein [before Clinical trials; 1 month, 2 months, 3 months, 6 months after randomization]

      24-hour urinary protein quantitative, urinary microprotein

    2. Change in renal function of the patients [before Clinical trials; 1 month, 2 months, 3 months, 6 months after randomization]

      blood chemistry

    3. change of lymphocyte subsets [before Clinical trials; 1 month, 2 months, 3 months, 6 months after randomization]

      including Th1 cells, Th2 cells, Th17 cells, cytokines (IL-16, IL-10, IL-17, etc.)

    4. change of immunoglobulin + complement [before Clinical trials; 1 month, 2 months, 3 months, 6 months after randomization]

      immunoglobulin + complement

    5. change of urine red blood cells [before Clinical trials; 1 month, 2 months, 3 months, 6 months after randomization]

      red blood cells routine urine

    Secondary Outcome Measures

    1. Change of blood pressure [before Clinical trials; 1 month, 2 months, 3 months, 6 months after randomization]

      blood pressure

    2. change of BMI(Body Mass Index) [before Clinical trials; 1 month, 2 months, 3 months, 6 months after randomization]

      calculated by dividing weight in kilograms by height in meters squared( kg/m^2)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Years to 14 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. For children diagnosed with purpura nephritis, the diagnostic criteria for purpura nephritis shall refer to the 2016 edition of Evidence-based Guideline for diagnosis and Treatment of Purpura Nephritis published by the Nephrology Group of The Chinese Medical Association Pediatrics Branch, specifically as follows: Hematuria and/or proteinuria occur within 6 months of the course of allergic purpura. The diagnostic criteria for hematuria and proteinuria are as follows: A. Hematuria: gross hematuria or ≥3 RBC/high-power field (HP) under 3 times of microscope within 1 week. B. Proteinuria: if meeting any of the following conditions: 3 routine urine tests within 1 week qualitatively indicate positive urine protein; 24h quantitative urine protein

    150 mg or urine protein/creatinine (mg/mg)>0.2; Urinary microalbumin was higher than normal for 3 times within 1 week. Very few children in the acute course of allergic purpura 6 months later, recurrent purpura, hematuria and/or proteinuria for the first time, should be sought for renal biopsy, such as IgA mesangial mesangial proliferative glomerulonephritis, can still be diagnosed as purpura nephritis.

    1. 24-hour urinary protein quantification of 0.5 to 1.0g/1.73m2, and the total amount does not exceed 1.0g (to be quantified in non-infectious conditions);

    2. Age: 6-14 years old;

    3. Normal renal function: eGFR≥90ml/min/1.73m2;

    4. Other manifestations of allergic purpura: skin purpura, abdominal pain, blood stool and joint swelling and pain have been relieved, and the use of hormone or immunosuppressive agents has been stopped for 2 weeks.

    Exclusion Criteria:
    1. Abnormal ophthalmic examination (fundus, visual field, photosensitivity);

    2. Combined with gross hematuria;

    3. Serious diseases of the heart, liver and other important organs, as well as diseases of the blood and endocrine system;

    4. Patients who are known to be allergic to any component of Locust and wolfberry yellow or ACEI/ARB;

    5. Patients who have participated in other clinical trials within three months before enrollment;

    6. The investigator judged that the patient was not fit to participate in the study;(7) renal purpura nephritis wear results indicate Ⅲ magnitude or hints chronic purpura nephritis.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Children Hospital of Zhejiang University School of Medicine Hangzhou Zhejiang China 310006
    2 Children's Hospital, Zhejiang University School of Medicine Hangzhou Zhejiang China

    Sponsors and Collaborators

    • The Children's Hospital of Zhejiang University School of Medicine

    Investigators

    • Study Chair: Mao Jianhua, Children's Hospital, Zhejiang University School of Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Mao Jianhua, The Children's Hospital of Zhejiang University School of Medicine, The Children's Hospital of Zhejiang University School of Medicine
    ClinicalTrials.gov Identifier:
    NCT04623866
    Other Study ID Numbers:
    • CXPJJH12000003-202017
    First Posted:
    Nov 10, 2020
    Last Update Posted:
    Nov 10, 2020
    Last Verified:
    Nov 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 10, 2020