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The effect of pentoxifylline 400 mg on anemia control and decreasing the dose of erythropoietin

Evaluation of the effect of pentoxifylline 400 mg on anemia control and decreasing the dose of erythropoietin in chronic hemodialysis patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180122038471N1
Enrollment
16
Registered
2018-02-08
Start date
2018-01-05
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Anemia. Refractory anemia, unspecified

Interventions

Intervention 1: Intervention group: 400 mg pentoxifylline pill, made in Iran, once daily for 12 weeks, with an appropriate dosage of intravenous erythropoietin for each patient diagnosed by physician

Sponsors

Urology Research Centre, Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: GFR less than 15 Have been under hemodialysis for at least 3 months Performing regular hemodialysis 3 times a week Having an iron saturation of more than 30% and ferritin more than 500 Dialysis adequacy criteria: Kt/V greater than 1/2 Have an arteriovenous fistula or a pacifier for hemodialysis Hemoglobin less than 11 in at least 2 consecutive tests within a month

Exclusion criteria

Exclusion criteria: History of bleeding in a recent month History of infection leading to hospitalization in a recent month Use of theophylline and androgens Intolerance to drug use in oral form Patient dissatisfaction The patient has undergone blood transfusion or B12 administration for any reason during the last 3 months. The presence of any underlying illness that justifies anemia, including thyroid and parathyroid dysfunction, hemoglobinopathy and malnutrition, and ... Hemorrhagic retinopathy The presence of coronary artery disease in the last 3 months

Design outcomes

Primary

MeasureTime frame
Hemoglobin level. Timepoint: At the beginning of the study (before the intervention) and 4, 8 and 12 weeks after the intervention. Method of measurement: Blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamira Rahimi

Rasht University of Medical Sciences

urc1384@yahoo.com+98 13 3352 5259

Outcome results

None listed

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