Clinical Trials Logo

Clinical Trial Summary

This study is a multicentric, prospective, randomized, double blind, placebo controlled trial compared the efficacy of 6 months vs. 3 months of initial prednisolone therapy in decreasing the incidence of FRNS with steroid-sensitive nephrotic syndrome in children age 1 year up to 6 years. Three months tapering prednisolone or placebo are administrated follow by open-label 3 months standard prednisolone therapy.The cumulative incidence of FRNS and adverse events for one year were evaluated in the 3-month and 6-month groups.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04536181
Study type Interventional
Source Children's Hospital of Fudan University
Contact
Status Withdrawn
Phase Phase 3
Start date January 1, 2021
Completion date October 1, 2022

See also
  Status Clinical Trial Phase
Recruiting NCT05786768 - Efficacy and Safety of Obinutuzumab Versus Rituximab in Childhood Steroid Dependant and Frequent Relapsing Nephrotic Syndrome Phase 2/Phase 3
Recruiting NCT06065852 - National Registry of Rare Kidney Diseases
Recruiting NCT04713410 - Comparison of Relapse Rate After 12 Weeks Verses 20 Weeks Steroid Therapy for the Management of First Episode of Steroid Sensitive Nephrotic Syndrome N/A
Completed NCT04783675 - Efficacy and Safety of Rituximab in the First Episode of Pediatric Idiopathic Nephrotic Syndrome Phase 2
Not yet recruiting NCT05850546 - Rituximab in the First Episode of Paediatric Nephrotic Syndrome Phase 3