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Levothyroxine in Nephrotic syndrome

Comparing the effect of adding levothyroxine to steroids versus steroids alone on reducing the duration of relapse requiring hospitalization in children with nephrotic syndrome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201112049368N2
Enrollment
82
Registered
2024-05-30
Start date
2022-11-23
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nephrotic Syndrome. Nephrotic syndrome

Interventions

Intervention 1: Intervention group: The intervention group will be treated from the time of hospitalization due to recurrence with an oral levothyroxine tablet manufactured by Iran Hormone Company at

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 12 Years

Inclusion criteria

Inclusion criteria: idiopathic nephrotic syndrome Relapse requiring hospitalization serum TSH grater than 5.5 mIU/L

Exclusion criteria

Exclusion criteria: congenital nephrotic syndrome Secondary nephrotic syndrome GFR less than 60 ml/min/1.73 m2 confirmed hypothyroidism before the diagnosis of nephrotic syndrome

Design outcomes

Primary

MeasureTime frame
Relapse duration. Timepoint: during the whole period of study. Method of measurement: Urinary dipstick test.

Secondary

MeasureTime frame
Cumulative dose of prednisolon. Timepoint: At the incidence of remission. Method of measurement: recorded medical instructions and nursing report.;Cumulative dose of albumin. Timepoint: During relapses. Method of measurement: recorded medical instructions and nursing report.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmin Taheri

Artesh University of Medical Sciences

amin.taheri2731@gmail.com+98 51 5422 2821

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026