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Effect of pentoxifylline on inflammatory factors and quality of life in hemodialysis patients

Effect of pentoxifylline on inflammatory factors and quality of life in hemodialysis patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170609034406N3
Enrollment
100
Registered
2019-09-21
Start date
2019-04-21
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

End Stage Renal Disease. Chronic kidney disease, stage 5

Interventions

Intervention 1: Intervention group: The treatment group consists of 50 patients receiving 400 mg orally of Pentoxifylline daily for 3 months. Intervention 2: Control group consisted of 50 patients rec

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: CRP>1 Age over 18 years Initiate hemodialysis for at least 3 months and three times a week Ability to understand and sign a consent form Properly functioning arteriovenous fistula or catheter Dialysis adequacy above 1.2

Exclusion criteria

Exclusion criteria: Pregnancy The presence of any chronic,active,uncontrolled or severe chronic inflammatory disease(autoimmune disease,connective tissue disease,malignancy,HIV,liver disaese and pulmonary disease) The presence of chronic infection or the occurrence of acute infection in a recent month Hemoglobin is less than 10g/dL Concurrently presence in another trial(drug or supplement) A medical history(such as heart attack or brain injury)or sergical in the last 3 months Symptoms of malabsorption Bleeding disorders(Includes coagulopathies)or high risk of bleeding Change in diet in the last 1 month Abuse of alcohol and other substances that cause dependence

Design outcomes

Primary

MeasureTime frame
Serum level of TNF-a. Timepoint: Before intervention. At the end of the intervention. Method of measurement: ELISA kit.;Serum level of CRP. Timepoint: Before intervention. At the end of the intervention. Method of measurement: ELISA kit.

Secondary

MeasureTime frame
Quality of life. Timepoint: Before intervention. At the end of the intervention. Method of measurement: Standard questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfshin Gharekhani

Tabriz University of Medical Sciences

gharekhania@tbzmed.ac.ir+98 41 3230 5351

Outcome results

None listed

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