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Calcitriol in the Treatment of Immunoglobulin A Nephropathy

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00862693
Enrollment
40
Registered
2009-03-17
Start date
2009-03-31
Completion date
2011-03-31
Last updated
2011-02-17

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

Conditions

Autoimmune Diseases, Glomerulonephritis

Keywords

Immunoglobulin A, Antibodies, treatment

Brief summary

Immunoglobulin A (IgA) nephropathy is the common primary glomerulonephritis in the world. Much literature suggests that vitamin D and its analogs have profound effects on immune system function and glomerular mesangial cell proliferation. Therefore, the investigators plan to conduct a randomized clinical study to evaluate the efficacy of Calcitriol in the treatment of IgA nephropathy. Forty patients with biopsy-proven IgA nephropathy will be recruited. They will be randomized to Calcitriol for six months or no treatment. Proteinuria, renal function, serum and urinary inflammatory markers will be monitored. This study will explore the potential anti-proteinuric and anti-inflammatory effects of Calcitriol in the treatment of IgA nephropathy, which has no specific treatment at present.

Interventions

DRUGCalcitriol

0.5ug/Biw

Sponsors

Peking University First Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Aged 18-65 years * Biopsy-confirmed IgA nephropathy * Proteinuria \> 0.8 g/day in 3 consecutive samples within 12 weeks despite ACE inhibitor or angiotensin receptor blocker treatment for at least 3 months or estimated glomerular filtration rate \< 60 ml/min/1.73m2 * Corrected serum calcium level \< or = 2.45 mmol/l * Willingness to give written consent and comply with the study protocol

Exclusion criteria

* Pregnancy, lactating or childbearing potential without effective method of birth control * Severe gastrointestinal disorders that interfere with their ability to receive or absorb oral medication * History of malignancy, including leukemia and lymphoma within the past 2 years * Systemic infection requiring therapy at study entry * Any other severe coexisting disease such as, but not limited to, chronic liver disease, myocardial infarction, cerebrovascular accident, malignant hypertension * History of drug or alcohol abuse within past 2 years * Participation in any previous trial on paricalcitol * Patients receiving treatment of vitamin D and/or its analogue for other medical reasons within the past 3 months * Patients receiving treatment of corticosteroid * On other investigational drugs within last 30 days * History of a psychological illness or condition such as to interfere with the patient's ability to understand the requirement of the study * History of non-compliance * Known history of sensitivity or allergy to paricalcitol or other vitamin D analogs

Design outcomes

Primary

MeasureTime frameDescription
decline of urine protein12 months treatmentanalysis urine protein after 12 months treatment

Countries

China

Contacts

Primary ContactHong Zhang, Prof
hongzh@bjmu.edu.cn+86-10-66551122-2288

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026