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Effect of thymosin 1 on recurrent minor nephrotic syndrome in adults

A prospective, randomized controlled trial of oral prednisone combined with thymosin 1 in recurrent adult patients with minimal lesions nephrotic syndrome

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100041655
Enrollment
Unknown
Registered
2021-01-01
Start date
2020-12-30
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

Minimal change nephrotic syndrome

Interventions

Oral prednisone:oral prednisone
Oral prednisone combined with thymosin 1 group:Thymosin 1 was injected

Sponsors

Affiliated Hospital of Guangdong Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The patients who voluntarily participated in this study and signed the informed consent; 2. Patients aged 18-70 years; 3. Patients diagnosed as minimal change nephrotic syndrome by pathology; 4. Patients with complete remission and recurrence (urinary protein > 3.5g/d or urinary protein / creatinine 3500mg / g) after standard hormone therapy.

Exclusion criteria

Exclusion criteria: 1. Those patients with severe infection; 2. Patients with secondary glomerular diseases; 3. Patients with severe gastrointestinal complications or other reasons who can not accept oral drug treatment; 4. Those patients with hormone and Thymosin contraindications and intolerance; 5. Patients with mental disorder and poor compliance; 6. Patients with severe primary diseases such as cardiovascular, cerebrovascular, endocrine and hematopoietic system; 7. Pregnant and lactating women; 8. The patients who met the inclusion criteria of the study were withdrawn from the study due to their personal wishes.

Design outcomes

Primary

MeasureTime frame
The recurrence rate;

Secondary

MeasureTime frame
Infection rates;

Countries

China

Contacts

Public ContactYao Cuiwei

Guangdong Medical University

Yaocuiwei826@163.com+86 13671458718

Outcome results

None listed

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