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Efficacy of Pentoxifylline in diabetic nephropathy

Phase 3
Conditions
Condition 1: Type 2 Diabetes. Condition 2: Diabetic Nephropathy.
Type 2 diabetes mellitus
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N00-N08
Registration Number
IRCT20190806044451N2
Lead Sponsor
Zanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Type 2 diabetic patients treated with insulin and oral agents
GFR above 30 cc / min / 1.73 m2
albuminuria above 300 mg/g

Exclusion Criteria

Patient dissatisfaction
Type 1 diabetes
Pentoxifylline allergy
Chronic heart failure
Uncontrolled hypertension
Other medicines that affect albuminuria
Cerebral hemorrhage
Extensive retinal hemorrhage
ESRD, GFR <30
Pregnancy
Hyperkalemia (high potassium) 5.5 before or during the study)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Random Urin Albumin/Creatinine. Timepoint: 3 months before intervention and before starting pentoxifylline and 3 months after starting pentoxifylline. Method of measurement: Lab test.
Secondary Outcome Measures
NameTimeMethod
Creatinin. Timepoint: Before starting pentoxifylline and 3 months after starting pentoxifylline. Method of measurement: Lab test.;Hemoglobin A1c. Timepoint: Before starting pentoxifylline and 3 months after starting pentoxifylline. Method of measurement: Lab test.;Blood pressure. Timepoint: Before starting pentoxifylline and 3 months after starting pentoxifylline. Method of measurement: Sphygmomanometer.;Body mass index. Timepoint: Before starting pentoxifylline and 3 months after starting pentoxifylline. Method of measurement: meter & Balance.;Fasting blood sugar (FBS). Timepoint: Before starting pentoxifylline and 3 months after starting pentoxifylline. Method of measurement: Lab test.;Pentoxifylline Complications. Timepoint: Before starting pentoxifylline and 3 months after starting pentoxifylline. Method of measurement: History taking.
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