Prednisolone Trial in Children Younger Than 4 Years
关键词
抽象
描述
Trial Registration Note:This trial was initially registered in the Indian Registry (list the number) on (date) prior to enrolling participants. The present listing shows this status of currently enrolling. New sites in the United States are expected to open within the coming year. At that time the answers to some questions, such as "Studies FDA regulated drug" will change because the basis for FDA regulation will reside on the presence of US sites and the use of US manufactured drug, whereas at this time the drug is not of US manufacture, and the trial is not currently conducted in the United States. This registration is being posted at this time to prepare to meet United States FDAAAA registration requirements.
Nephrotic syndrome is a common renal disorder in children characterized by proteinuria, hypoalbuminemia and edema. The long-term prognosis for steroid-sensitive nephrotic syndrome is excellent for resolution of disease and maintenance of renal function. About 80% patients with steroid-sensitive nephrotic syndrome will relapse one or more times, requiring repeated treatment with corticosteroids. Of these, 50-60% show frequent relapses or steroid dependence and require therapy with long-term corticosteroids and other medications. Patients with multiple relapses are at risk for life-threatening infections, malnutrition and thrombotic episodes. They are also likely to show serious side effects of long-term steroid therapy and those related to use of other medications, including toxicity to bone marrow, gonads, central nervous system and kidneys. Repeated relapses also result in multiple hospitalizations and school absence. Strategies effective in reducing relapse rates and proportion of patients with frequent relapses or steroid dependence shall therefore be extremely valuable in improving the long-term management of nephrotic syndrome.
Based on information from multiple studies that prolonged duration of initial therapy beyond 8-weeks reduced the risk of an early relapse and lowered frequency of subsequent relapses, it is agreed upon that the initial therapy with prednisolone should continue for 12 weeks (3 months), administered daily for a duration of 6 weeks, and then on alternate days for another 6 weeks. However, the optimal dose and duration of corticosteroid therapy remains to be determined. Data from various prospective studies, systematically reviewed in the Cochrane Registry, suggests the beneficial effects of prolongation of treatment beyond 3 months, with benefit seen up to 6-months. However, the advantages of extending therapy from 3- to 6-months are not unambiguous; there are also concerns of the corticosteroid toxicity with the latter regimens. Recent placebo controlled trials reported in 2013, including from this center, suggest that extending initial prednisolone treatment from 3 months to 6 months, with or without an increase in cumulative dose, does not influence the course of disease in children with nephrotic syndrome. However, in the study conducted in India, we found that prolonged therapy was useful in postponing the first relapse, and was associated with an insignificantly decreased risk of frequent relapses, in the subgroup of children younger than 4 years. Since the subgroups were not defined a priori, a prospective study is required to clarify the efficacy of this intervention in young patients.
Further, the lack of clarity regarding disease pathogenesis makes the administration of corticosteroid therapies largely empirical. While clear insight into the pathogenic pathways targeted by prednisolone is lacking, there is some evidence that disease remission is associated with down regulation of T cell activation, altered B-T cell crosstalk, upregulation of T helper type 1(Th1) and/or T regulatory compartments.
This present study proposes to examine the benefits of prolongation of initial therapy of idiopathic nephrotic syndrome from the current standard of 3 to 6 months among children younger than 4-yr-old an onset of disease. Prolongation of treatment at the first episode would have considerable promise, if found effective in reducing future relapses and without concomitant risks of corticosteroid toxicity. The proposal also aims to examine the proportions of T and B lymphocyte subsets in 20 patients with the initial episode of nephrotic syndrome. The evaluation shall be conducted at onset of disease, following prednisolone induced disease remission, and at one year from randomization or at first relapse of the disease to determine differences in the immune profiles at different stages of the disease. Apart from improving our knowledge of pathogenesis of nephrotic syndrome, this approach shall enhance our understanding of the immunological alterations influenced by therapy.
日期
| 最后验证: | 06/30/2019 |
| 首次提交: | 03/16/2017 |
| 提交的预估入学人数: | 05/02/2017 |
| 首次发布: | 05/04/2017 |
| 上次提交的更新: | 06/30/2019 |
| 最近更新发布: | 07/04/2019 |
| 实际学习开始日期: | 06/30/2015 |
| 预计主要完成日期: | 10/30/2020 |
| 预计完成日期: | 10/30/2021 |
状况或疾病
干预/治疗
Drug: Intervention: Prednisolone
相
手臂组
| 臂 | 干预/治疗 |
|---|---|
| Experimental: Intervention: Prednisolone Drug: 12- Weeks of Prednisolone Therapy Subjects will add an additional 12 weeks of Prednisolone to follow pre-randomization standard of care prednisolone. Post randomization Prednisolone therapy of 30 mg/m2 on alternate days for 4 weeks, 20 mg/m2 on alternate days for 4 weeks, and 10 mg/m2 on alternate days for 4 weeks | Drug: Intervention: Prednisolone Prednisolone for 12 weeks as follows 30 mg/m2 on alternate days for 4 weeks 20 mg/m2 on alternate days for 4 weeks 10 mg/m2 on alternate days for 4 weeks |
| No Intervention: No intervention Subjects will NOT receive 12-weeks of additional Prednisolone therapy following randomization |
资格标准
| 有资格学习的年龄 | 1 Year 至 1 Year |
| 有资格学习的性别 | All |
| 接受健康志愿者 | 是 |
| 标准 | Inclusion Criteria: 1. Idiopathic, steroid-sensitive, first episode of nephrotic syndrome 2. Age 12 months up to 48 months 3. Written informed consent Exclusion Criteria 1. Nephrotic syndrome known to be secondary to a systemic disorder, e.g., Immunoglobulin A (IgA) nephropathy, systemic lupus erythematosus, Henoch Schonlein purpura, vasculitis, , hepatitis B or Alport syndrome. 2. Persistent estimated glomerular filtration rate (GFR) <75 ml/min/1.73 m2, 3. Therapy with prednisolone for prior episodes of nephrotic syndrome, 4. Therapy with corticosteroids in the past 3 months, in a dose more than 1 mg/kg for >14 days for any other reason, 5. Corticosteroid therapy for initial episode of nephrotic syndrome prior to randomization varying from pre-specified protocol on more than 14 days, 6. Patients who show relapse during the first 3 months of pre-randomization corticosteroid therapy for nephrotic syndrome, 7. Unclear treatment history, 8. Gross hematuria, 9. Patients with initial steroid resistance, 10. Participation in any other drug study during the course of this study. 11. Participation in more than one study without approval from the researchers involved in each study, |
结果
主要结果指标
1. Relapse of nephrotic syndrome during 12 months after randomization [12 month period following randomization]
次要成果指标
1. Number of relapses during 12 months follow up [12 month period following randomization]
2. Time to first relapse (days) [12 month period following randomization]
3. Occurrence of frequent relapses of nephrotic syndrome during 12 months from randomization [12 month period following randomization]
4. Cumulative prednisolone [or corticosteroid equivalent] received during 12 month period from randomization [12 month period following randomization]
5. The use of steroid-sparing medications [12 month period following randomization]
6. Adverse events during 12-month period after randomization [12 month period following randomization]
7. Change in anthropometry and growth velocity during 12-month period after randomization [12 month period following randomization]
其他成果措施
1. In a subgroup of 20 patients, the proportions of the following cell subsets, at baseline and at 6 and 12 months after randomization and at first relapse [12 month period following randomization]
2. Relapse of nephrotic syndrome during 24 months after randomization [24 month period following randomization]
3. Number of relapses during 24 months follow up [24 month period following randomization]
4. Time to first relapse (days) [24 month period following randomization]
5. Occurrence of frequent relapses of nephrotic syndrome during 24 months from randomization [24 month period following randomization]
6. Cumulative prednisolone [or corticosteroid equivalent] received during 24 month period [24 month period following randomization]
7. Relapse of nephrotic syndrome during 12 months after randomization in boys compared to girls [12 month period following randomization]
8. Relapse of nephrotic syndrome during 12 months after randomization in patients <2-yr-old at randomization compared to older patients [12 month period following randomization]
9. Relapse of nephrotic syndrome during 12 months after randomization in Indian patients compared to those in the USA [12 month period following randomization]
10. Number of relapses during 12 months follow up in boys compared to girls [12 month period following randomization]
11. Number of relapses during 12 months follow up in patients <2-yr-old at randomization compared to older patients [12 month period following randomization]
12. Number of relapses during 12 months follow up in Indian patients compared to those in the USA [12 month period following randomization]
13. Time to first relapse (days) in boys compared to girls [12 month period following randomization]
14. Time to first relapse (days) in patients <2-yr-old at randomization compared to older patients [12 month period following randomization]
15. Time to first relapse (days) in Indian patients compared to those in the USA [12 month period following randomization]
16. Occurrence of frequent relapses of nephrotic syndrome during 12 months from randomization in boys compared to girls [12 month period following randomization]
17. Occurrence of frequent relapses of nephrotic syndrome during 12 months from randomization in patients <2-yr-old at randomization compared to older patients [12 month period following randomization]
18. Occurrence of frequent relapses of nephrotic syndrome during 12 months from randomization in Indian patients compared to those in the USA [12 month period following randomization]
19. Cumulative prednisolone [or corticosteroid equivalent] received during 12 month period in boys compared to girls [12 month period following randomization]
20. Cumulative prednisolone [or corticosteroid equivalent] received during 12 month period in patients <2-yr-old at randomization compared to older patients [12 month period following randomization]
21. Cumulative prednisolone [or corticosteroid equivalent] received during 12 month period in Indian patients compared to those in the USA [12 month period following randomization]
