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Effect of pentoxifyllin on microalbominuria in patients with diabetic nephropathy

Effect of pentoxifyllin on microalbominuria in patients with diabetic nephropathy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201312212417N15
Enrollment
40
Registered
2014-02-23
Start date
2011-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Diabetic nephropathy. Diabetic nephropathy

Interventions

Placebo
Treatment - Drugs
Placebo tablet: three times a day for 6 months manufactured by amin company
Intervention 1: Placebo tablet: three times a day for 6 months manufactured by amin company. Intervention 2: Pentoxifyllin tablet: 400 mg three times a day for 6 month manufactured by amin company.
Pentoxifyllin tablet: 400 mg three times a day for 6 month manufactured by amin company

Sponsors

Vice Chancellor for Research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1.Estimated glomerular filtration rate: higher than 60 mL/min/1.73 m2; 2.Blood pressure: less than 140/90 mmHg by using anti hypertensive drugs in the last six month 3.protein intake: less than 0.8gr/kg/d; 4.controlled blood glucose (glycosylated hemoglobin: less than 8%); 5.Spot urine albumin to creatinine ratio: less than 300 mg/g in 3 consecutive measurements during a 3 months screening period. exclusion criteria: 1.Myocardial infarction; 2.Stroke; 3.Retinal hemorrhage in last 6 months; 4.abnormal liver function tests ; 5.Congestive heart failure (New York Heart Association class III or IV); 6.Obstructive uropathy 7.Active malignancy; 8.Patients who could not discontinue immunosuppressive or nonsteroidal anti inflammatory drugs; 9.Pregnant or breast feeding women 10. changes in anti-hypertensive drugs 11.other cause of proteinuria

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Albumin/creatinine ratio of random urine sample. Timepoint: At begining, three and six months later. Method of measurement: Photometric method (mg/g).;Glomerular filtration rate. Timepoint: At begining and the end of study. Method of measurement: Modification of Diet in Renal Disease (MDRD formula).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.marzieh hoseinbalam

Isfahan University of Medical Sciences

drhoseinbalam@yahoo.com+98 31 1625 5555

Outcome results

None listed

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