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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03015974
Other study ID # 2015[992]
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2016
Est. completion date December 2024

Study information

Verified date December 2023
Source Peking University First Hospital
Contact Xuhui Zhong, Dr.
Phone 8613683556856
Email xuhui7876@126.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study tries to identify the safe and effective treatment option for IgA nephropathy in children. Investigators will perform prospective registration study among 25 pediatric nephrology medical centers in China.


Description:

A total of 1200 patients diagnosed as primary IgA nephropathy with nephrotic proteinuria will be enrolled among 25 pediatric nephrology medical centers nationwide, according to the following protocol. 1. Establishment of registration database online. 2. Participants will be enrolled according to the inclusion criteria and exclusion criteria. 3. The following data will be collected prospectively, including demographic data, clinical symptoms, physical examination, laboratory examination, renal pathology, treatment protocol and follow-up. 4. SPSS software (version 14.0; SPSS, Inc., Chicago, IL, USA) will be used for statistical analysis. P value less than 0.05 will be considered significant.


Recruitment information / eligibility

Status Recruiting
Enrollment 1200
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group 1 Month to 18 Years
Eligibility In-patients will be enrolled with the following criteria. Inclusion Criteria: - Clinical diagnosis of primary IgA nephropathy. - Presenting with nephrotic proteinuria, defined as 24-hour urinary protein>50mg/kg, or UPC>2.0 mg/mg. - Informed consent must be signed. Exclusion Criteria: - Diagnosed as secondary renal diseases, including lupus nephritis, purpura nephritis, hepatitis B virus associated nephritis, etc.

Study Design


Intervention

Drug:
Corticosteroid

Cyclophosphamide

Mycophenolate mofetil

Dipyridamole

ACE Inhibitor or Angiotensin receptor antagonist


Locations

Country Name City State
China Peking University First Hospital Beijing

Sponsors (25)

Lead Sponsor Collaborator
Peking University First Hospital Beijing Children's Hospital, Capital Institute of Pediatrics, China, Central South University, Chengdu Women's and Children's Central Hospital, Children's Hospital of Chongqing Medical University, Children's Hospital of Hebei Province, First Affiliated Hospital, Sun Yat-Sen University, Fuzhou General Hospital, Guangzhou First People's Hospital, Guangzhou Women and Children's Medical Center, Hunan Children's Hospital, Jiangxi Province Children's Hospital, Nanjing Children's Hospital, Nanjing PLA General Hospital, Second Affiliated Hospital of Wenzhou Medical University, Shandong Provincial Hospital, Shanghai Children's Hospital, The Children's Hospital of Zhejiang University School of Medicine, The First Hospital of Jilin University, The First People's Hospital of Yunnan, Tianjin Children's Hospital, Tongji Hospital, Wuhan Women and Children's Medical Center, Xian Children's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement of proteinuria Complete remission is defined as 24-hour urine protein<150mg or UPC<0.3 g/g with normal kidney function. Partial remission is defined as urine protein decreased by more than 50% with normal renal function. Two years
Primary Renal dysfunction Renal dysfunction is defined as eGFR declined by more than 50%. Two years
Primary Hypertension Hypertension is defined as blood pressure higher than age-specific average level. Use of antihypertensive drugs will be recorded. Two years
Secondary End stage renal disease(ESRD) ESRD is defined as eGFR<15ml/min/1.73m2, initiation of long-term dialysis or kidney transplant. Two years
Secondary Mortality Death of participants will be recorded. Two years
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