Cohort Study on Traditional Chinese Medicine Diagnosis and Treatment of Children With Henoch-Schonlein Purpura Nephritis
CSTCMDTCHSPN
1 other identifier
observational
600
1 country
1
Brief Summary
Henoch-Schonlein purpura nephritis(HSPN) is one of the most common secondary glomerulonephritis in children. A large, prospective, multicenter cohort study is being conducted in three institutions. Eligible Henoch-Schönlein purpura nephritis children will be classified as the experimental group (n=300) and the control group (n=300) based on the interventions they receive. Patients taking Chinese herbal formula will be in the experimental group, and those taking Western medicine will be in the control group. The entire study will last 60 weeks, including a 12-week observation period and a followup at 12 months.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2016
Typical duration for all trials
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 17, 2016
CompletedFirst Posted
Study publicly available on registry
August 25, 2016
CompletedStudy Start
First participant enrolled
September 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2020
CompletedMarch 4, 2019
March 1, 2019
2.5 years
August 17, 2016
March 1, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Urine protein
1. Recovery:Urine protein(-). 2. Marked effect:Urine protein reduces by 2'+'. 3. Effective:Urine protein reduces by 1'+'. 4. Ineffective:Urine protein has no changes.
2 weeks
24-hour urinary protein excretion
1. Recovery:24-hour urinary protein excretion is normal. 2. Marked effect:24-hour urinary protein excretion reduction is larger than 50%. 3. Effective:24-hour urinary protein excretion reduction is smaller than 50%. 4. Ineffective:24-hour urinary protein excretion has no changes.
2 weeks
Urine erythrocyte
1. Recovery:Urine erythrocyte is normal. 2. Marked effect:Urine erythrocyte reduction is larger than 50%. 3. Effective:Urine erythrocyte reduction is smaller than 50%. 4. Ineffective;Urine erythrocyte has no changes.
2 weeks
Creatinine clearance rate and Serum creatinine
Diagnostic criteria of chronic renal failure: 1. Creatinine clearance rate\<80ml/min; 2. Serum creatinine\>133μmol/L; 3. The patient who have a history of chronic kidney diseases or systemic diseases involving kidney.
1 year
Secondary Outcomes (2)
Number of patients with hormone therapy
3 months
Number of patients with immunosuppressant therapy
3 months
Study Arms (2)
TCM intervention
Participants with HSPN of the Heat-Toxin type will take the Qi-Ji Shen-Kang formula. HSPN patients of the Wet-Heat type will take the Zhu-Bai formula. Those of Qi-Deficiency with Blood-Stasis type will take the Yu-Shen formula.
WM conventional intervention
The WM conventional intervention, recommended by the Chinese Medical Association's (CMA) Scientific Statement, includes angiotensin-converting enzyme (ACE) inhibitor, adrenergic receptor binder (ARB), adrenal cortical hormone, Tripterygium wilfordii polyglycosidium and an immunosuppressant.
Interventions
Qi-Ji Shen-Kang formula:15g of field thistle,10g of common edelweiss herb,10g of spreading hedyotis herb,10g ofYunnan manyleaf Paris rhizome,10g of hairyvein agrimonia herb,10g of the root bark of the tree peony,15g of root of red rooted salvia, and 15g ofmembranous mikvetch root.Zhu-Bai formula:10g of glabrous greenbrier rhizome,5g of Chinese atractylodes rhizome,10g of amur corktree bark,10g of common edelweiss her),10g of field thistle,10g of lalang grass rhizome,10g of garden burnet root,5g of longbract cattail pollen,5g of rehmanniae radix, and 5g of Chinese angelica root.Yu-Shen formula:15g of membranous mikvetch root,10g of heterophylla falsestarwort root,10g of field thistle,10g of cogongrass rhizome,10g of spreading hedyotis herb,10g of root of red rooted salvia,10g of fresh root of rehmannia,10g of Asian puccoon,10g of wormwoodlike motherwort herb,10g of common cockscomb inflorescence,10g of gordon euyale,10g of root bark of the tree peony, and 5g of licorice root.
prednisone at a dose of 1-1.5 mg/(kg·d) and Tripterygium wilfordii polyglycosidium at a dose of 1 mg/(kg·d). For each patient, the specific Western medicines used and their doses may be adjusted at the discretion of his or her physician, but the classes cannot be changed.
Eligibility Criteria
Children with purpura nephritis who are treated in Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, Shengjing Hospital of China Medical University and The First Hospital of China Medical University will be regarded as the objects of study.
You may qualify if:
- A diagnosis of HSPN as well as three major constitution types (Heat-Toxin, Wet-Heat, Qi-Deficiency with Blood-Stasis) according to WM and TCM.
- Age: 5 to 18 years old (including 5 and 18 year-olds).
- The clinical classification of HSPN includes isolated hematuria, insolated proteinuria, hematuria with proteinuria, and acute glomerulonephritis.
- The ability to provide detailed connection and complete a followup.
- The ability to understand and sign a written informed consent.
You may not qualify if:
- HSPN with renal insufficiency.
- A clinical classification of HSPN that includes nephritic syndrome, rapidly progressive glomerulonephritis and chronic glomerulonephritis.
- Suffering from serious complications, such as respiratory, digestive, hematological or liver diseases.
- Tumor, infectious diseases, or mental disorders.
- Allergic to TCM use.
- No prescribed medication, poor compliance, or incomplete data affecting the efficacy and safety of these judgments.
- A history of another clinical trial in the previous 2 weeks.
- No consent form signed.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Liaoning University of Traditional Chinese Medicinelead
- First Hospital of China Medical Universitycollaborator
- Shengjing Hospitalcollaborator
Study Sites (1)
Zhang Jun
Shenyang, Liaoning, 110032, China
Related Publications (1)
Zhang J, Lv J, Pang S, Bai X, Yuan F, Wu Y, Jiang H, Yang G, Zhang S. Chinese herbal medicine for the treatment of Henoch-Schonlein purpura nephritis in children: A prospective cohort study protocol. Medicine (Baltimore). 2018 Jun;97(24):e11064. doi: 10.1097/MD.0000000000011064.
PMID: 29901610DERIVED
Biospecimen
We will retain the blood of each patient to do some research of lncRNA with patients'permission.Try to find some relationship between lncRNA and HSPN disease.We also retain the urine and coated tongue to establish the biospecimen repository for our patients.When they grow up,these spicimens may help them to understand their bodies more correctly.
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
jun zhang, master
Affiliated Hospital of Liaoning University of Traditional Chinese Medicine
- STUDY DIRECTOR
jing lv, master
Affiliated Hospital of Liaoning University of Traditional Chinese Medicine
- PRINCIPAL INVESTIGATOR
shaoqing zhang, doctor
Affiliated Hospital of Liaoning University of Traditional Chinese Medicine
- PRINCIPAL INVESTIGATOR
guanqi yang, doctor
Affiliated Hospital of Liaoning University of Traditional Chinese Medicine
- PRINCIPAL INVESTIGATOR
shuang pang, doctor
Affiliated Hospital of Liaoning University of Traditional Chinese Medicine
- PRINCIPAL INVESTIGATOR
binyu wu, master
Shengjing Hospital
- PRINCIPAL INVESTIGATOR
yaoguo zhang, master
First Hospital of China Medical University
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 12 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
August 17, 2016
First Posted
August 25, 2016
Study Start
September 1, 2016
Primary Completion
March 1, 2019
Study Completion
May 1, 2020
Last Updated
March 4, 2019
Record last verified: 2019-03
Data Sharing
- IPD Sharing
- Will share
The Central Database of Clinical Evaluation of China Academy of Chinese Medicine Science