Skip to content

The effect of Pentoxifylline on C reactive protein level and dialysis adequacy

The effect of Pentoxifylline on C reactive protein level and dialysis adequacy in end stage renal disease patients under hemodialysis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013120715695N1
Enrollment
80
Registered
2014-01-28
Start date
2014-03-21
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

Condition 1: esrd. Condition 2: Ischemic Heart Disease. Chronic kidney Disease, stage 5 Angina pectoris, Acute myocardial infarction, Subsequent myocardial infarction, Certain current complications following acute myocardial infarction, Other acute ischaemic heart diseases, Chronic ischaemic heart disease,

Interventions

Intervention 1: Pentoxifylline Tab 400 mg daily 30 days in Intervention group. Intervention 2: Starch Tab daily in Control group.
Treatment - Drugs
Placebo
Pentoxifylline Tab 400 mg daily 30 days in Intervention group
Starch Tab daily in Control group

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: acceptance of written consent; End Stage Renal Disease; more than 15year; BMI between 15 - 35 Exclusion criteria: pentoxifylline use before study; no acceptance of written consent; abnormal LFT; hyper sensitivity reaction to pentoxifylline; active infection; recent malignancy; depression;recent ICH; recent retinal hemorrhage; dialysis period under 3 months

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
CRP. Timepoint: before and after receiving placebo or drug. Method of measurement: quantitative kit of CRP.

Secondary

MeasureTime frame
Dialysis Adequacy. Timepoint: before and after dialysis and before and after receiving placebo or drug. Method of measurement: KT/V: K ( cc/min ) x time ( min ) / urea volume ( cc ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Afsaneh Talayi

Amiralmomenin Hospital

amoozesh@arakmu.ac.ir+98 86 3417 3601

Outcome results

None listed

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