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
|
|
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
|
|
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. |