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CTRI Number  CTRI/2019/01/017091 [Registered on: 15/01/2019] Trial Registered Prospectively
Last Modified On: 11/02/2022
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   A study to examine whether giving steroids in low dose daily is more effective than if given on alternate days, in controlling disease activity in patients with frequently relapsing nephrotic syndrome 
Scientific Title of Study   Open label, randomized, controlled trial to compare the efficacy of daily therapy with low dose prednisolone versus standard therapy on alternate days in patients with frequently relapsing/steroid dependent nephrotic syndrome 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Aditi Sinha  
Designation  Assistant Professor 
Affiliation  All India Institute of Medical Sciences New Delhi 
Address  Room no 3055 Department of Pediatrics All India Institute of Medical Sciences New Delhi

South
DELHI
110029
India 
Phone  9899145489  
Fax    
Email  aditisinhaaiims@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Aditi Sinha  
Designation  Assistant Professor 
Affiliation  All India Institute of Medical Sciences New Delhi 
Address  Room no 3055 Department of Pediatrics All India Institute of Medical Sciences New Delhi

South
DELHI
110029
India 
Phone  9899145489  
Fax    
Email  aditisinhaaiims@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Aditi Sinha  
Designation  Assistant Professor 
Affiliation  All India Institute of Medical Sciences New Delhi 
Address  Room no 3055 Department of Pediatrics All India Institute of Medical Sciences New Delhi

South
DELHI
110029
India 
Phone  9899145489  
Fax    
Email  aditisinhaaiims@gmail.com  
 
Source of Monetary or Material Support  
Indian Council of Medical Research, V. Ramalingaswami Bhawan, Ansari Nagar, New Delhi, 110029 
 
Primary Sponsor  
Name  Indian Council of Medical Research 
Address  V. Ramalingaswami Bhawan, P.O. Box No. 4911 Ansari Nagar, New Delhi - 110029, India 
Type of Sponsor  Government funding agency 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Aditi Sinha  All India Institute of Medical Sciences  Division of Nephrology, Department of Pediatrics, All India Institute of Medical Sciences, Ansari Nagar
South
DELHI 
9899145489

aditisinhaaiims@gmail.com 
 
Details of Ethics Committee
Modification(s)  
No of Ethics Committees= 2  
Name of Committee  Approval Status 
AIIMS Ethics Committee  Approved 
AIIMS ethics committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: N040||Nephrotic syndrome with minor glomerular abnormality,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Prednisolone  Given daily at 0.15-0.2 mg/kg at 8.00 am for 18 months 
Comparator Agent  Prednisolone  Given on alternate days at dose of 0.5-0.6 mg/kg (standard treatment) for 18 months  
 
Inclusion Criteria  
Age From  2.00 Year(s)
Age To  18.00 Year(s)
Gender  Both 
Details  Children aged 2-18 yr with frequently relapsing or steroid dependent nephrotic syndrome
Written informed consent from parents 
 
ExclusionCriteria 
Details  Steroid resistant nephrotic syndrome
Congenital nephrotic syndrome
Nephrotic syndrome secondary to systemic disease (systemic lupus erythematosus, IgA nephropathy, infection with HIV or hepatitis B or C)
Estimated glomerular filtration rate below 60 ml/min/1.73 sq. m
Recent (during the last 6-months) therapy with long term alternate day prednisolone for >3-months, levamisole, cyclophosphamide or mycophenolate mofetil
History of therapy with cyclosporine, tacrolimus or rituximab
Significant steroid toxicity, as defined by BMI >2 SDS; stage 2 hypertension; cataract, glaucoma; fasting glucose levels >100 mg/dl; history of steroid psychosis 
 
Method of Generating Random Sequence   Stratified block randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
The proportions of patients with infrequent relapses  18 months 
 
Secondary Outcome  
Outcome  TimePoints 
Time to first relapse  18 months 
Time to frequent relapses  18 months 
Frequency of relapses  18 months 
Proportion of patients with sustained remission  18 months 
Proportion of patients with frequent relapses  18 months 
Frequency and types of infections  18 months 
Patients with corticosteroid related adverse events, including reduced growth velocity, obesity, cushingoid features, hirsutism, hypertension, cataract and glaucoma  18 months 
 
Target Sample Size   Total Sample Size="160"
Sample Size from India="160" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 3/ Phase 4 
Date of First Enrollment (India)   28/02/2019 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="4"
Months="3"
Days="15" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Open to Recruitment 
Publication Details   Not applicable 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Brief Summary
Modification(s)  

The management of patients with frequently relapsing nephrotic syndrome, a common morbidity of childhood, is difficult and requires close monitoring for adverse effects of disease and therapies. Therapy with prednisolone and alternative immunosuppressive agents is empirical without a clear understanding of the pathogenic pathways targeted by any of these interventions. While most patients respond promptly to corticosteroid therapy with remission of proteinuria, more than 80% relapse subsequently, either infrequently (20-25%) or frequently (50-60%). Relapses of nephrotic syndrome may be triggered by minor respiratory infections, allergic reactions or vaccination. Disease relapses are often associated with serious acute complications e.g., those related to anasarca, hypertension, life threatening infections (peritonitis, pneumonia, meningitis), thrombosis and malnutrition. Repeated courses of steroids lead to considerable medication related toxicity and morbidity. Reduction of relapse rates is therefore a major aim of long-term therapy of subjects with nephrotic syndrome.

Some preliminary studies have shown benefit of small daily dose prednisolone over standard alternate day regimen, but adequately powered randomized controlled trials are lacking.  In a previous study performed in this institute, authors compared twenty one patients given daily low dose prednisolone (LDP) with fourteen historic controls who were given standard alternate day therapy. They found  that long term therapy with a small daily dose of prednisolone can significantly reduce the number of relapses in patients with frequently relapsing nephrotic syndrome, and that the beneficial effect may continue even after its stoppage. The relapse rate in the LDP group during the treatment period was significantly lower than that observed during the preceding year when they were on standard alternate day therapy as well as that noted in the historical control group during the observation period of 18 months. In their study they found no side effects related to LDP [22]. Moreover, continued suppression of relapses after stoppage of treatment in some patients was a surprising observation, since other corticosteroid regimens do not affect the relapse rate once the drug is discontinued [23]. The side effects of glucocorticoids are numerous, well recognized and of great concern to the patients and their family. When unacceptable glucocorticoid related adverse events occur, these patients are considered for glucocorticoid sparing therapy [13, 14]. The assessment of glucocorticoid related adverse events is mostly based upon clinical observation rather than objective assessment [13].         

With this background, we propose to compare the safety and efficacy of therapy with daily prednisone in low doses (0.15-0.2 mg/kg) versus standard therapy (0.5-0.6 mg/kg) with prednisolone on alternate days (given daily for 5-7 days during episodes of infections) in maintaining disease remission over 24  months in patients with frequently relapsing nephrotic syndrome. If therapy with low dose prednisolone is found to be associated with sustained remission, fewer relapses and less significant adverse effects than therapy with prednisolone on alternate days, it would mark a paradigm shift in clinical practice recommendations of standard case management for patients with frequent relapses. This would have implications in terms of improved strategies for prevention of relapses and avoidance of serious adverse events including reduced growth rates, hypertension, cataracts, glaucoma, and psychological disorders, which would ultimately affect the outcome of children with FRNS. If the two are comparable in efficacy and safety, either agent may be offered, with parents being counseled regarding the relative efficacy and safety of each strategy.

During the study period of 24 months, patients are followed up regularly in the two limbs, at 3-monthly intervals, with clinical and laboratory monitoring as specified in the protocol, to monitor for various outcomes, including adverse effects of therapy, as well as control of disease. In view of the ongoing COVID-19 pandemic, as required by the circumstances, some of these visits may be replaced by (i) teleconsultations for history and compliance; (ii) review of urine protein diary and other relevant records over mobile apps; (iii) laboratory evaluations performed at standard local laboratories; (iii) physical examination, including  anthropometry and blood pressure, by local pediatrician; and (iv) ophthalmological evaluation for cataract and intraocular pressure by local ophthalmologist.

 
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