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Study of Sevelamer effect on nephropathic patients

Study of Sevelamer carbonate effects on hemoglobin A1c, blood glucose and inflammatory factors status in patients with diabetic kidney disease.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191111045401N1
Enrollment
48
Registered
2020-03-11
Start date
2019-07-23
Completion date
Unknown
Last updated
2020-03-24

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

Conditions

Diabetic nephropathy. Type 2 diabetes mellitus with diabetic nephropathy

Interventions

Intervention 1: Intervention group: diabetic nephropathic patients that given Sevelamer capsule 800 mg 3 times daily for two months before meal. Intervention 2: Control group: Diabetic nephropathic

Sponsors

Shahre-kord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years. Informed patient satisfaction diabetic nephropathy

Exclusion criteria

Exclusion criteria: Recently received treatment of hyperphosphatemia Have hypophosphatemia or hypercalcemia Pregnancy Known liver disease or active peptic ulcer5 Carbamazepine consumption

Design outcomes

Primary

MeasureTime frame
BS. Timepoint: Before the beginning of study and two month after using the sevelamer and placebo. Method of measurement: Biochemical assay using BTand optical absorption teqniqus and centrifugation of serum by sampler.;Inflamatory factors(ESR,CRP). Timepoint: Before the beginning of study and two month after using the sevelamer and placebo. Method of measurement: quantitative qualitative.;HBA1C. Timepoint: Before the beginning of study and two month after using the sevelamer and placebo. Method of measurement: Using the optical absorption method, we first use a kind of solution that binds to the glycosylated hemoglobin and produced color then we should mesure colored HB.;Inflamatory factor(ICAM,VCAM). Timepoint: Before the beginning of study and two month after using the sevelamer and placebo. Method of measurement: Elisa(measurement the serum level of Antibody).

Secondary

MeasureTime frame
Degree of systemic inflamation. Timepoint: Befour study and two month after using the drugs. Method of measurement: Quantitative rate of Inflamatory Factor.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShadi Botshekan

Shahre-kord University of Medical Sciences

mosadeghi@yahoo.com+98 38 3222 0016

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 17, 2026