Skip to content

The effect of pentoxifylline on diabetic microalbuminuria

Determination of the effect of pentoxifylline on microalbuminuria in type 2 diabetic patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190107042264N3
Enrollment
58
Registered
2020-12-16
Start date
2020-11-21
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Albuminuria in patients with diabetes Mellitus type II. Diabetes mellitus due to underlying condition with kidney complications

Interventions

Intervention 1: Intervention group: Patients in this group, in addition to receiving treatment for the underlying disease that is not altered by the intervention, are treated with pentoxifylline 400 m
Iran) once a day, after meals. This treatment lasts for 12 weeks. Intervention 2: Control group: Patients in this group, in addition to receiving treatment for the underlying disease that is not alter

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Type II Diabetic Patients Proteinuria more than 150mg/24hours Microalbuminuria of more than 20 mg albumin excretion in 24 hour urine

Exclusion criteria

Exclusion criteria: Patients Suffering from Diabetic Retinopathy Hypersensitivity to pentoxifylline Pregnancy Heart failure with Ejection fraction less than 35% Any acute or febrile illness one month before induction to study Use of spironolactone Use of Warfarin

Design outcomes

Primary

MeasureTime frame
Albuminuria. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: 24-hour urine collection.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShokouh Shayanpour

Ahvaz University of Medical Sciences

shayanpour-sh@ajums.ac.ir+98 61 3222 2114

Outcome results

None listed

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