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Pentoxifylline on Inflammatory Markers in Non-Diabetic Chronic Kidney Disease Patients

Effect of Pentoxifylline on Inflammatory Markers in Non-Diabetic Chronic Kidney Disease Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07315139
Enrollment
42
Registered
2026-01-02
Start date
2023-02-01
Completion date
2023-08-31
Last updated
2026-01-02

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

Conditions

Chronic Kidney Disease, Inflammatory Markers, Non-Diabetic, Pentoxifylline

Brief summary

This study aimed to determine the impact of Pentoxifylline on inflammatory biomarkers and the progression of chronic kidney disease in non-diabetic patients.

Detailed description

Chronic kidney disease (CKD) is a progressive condition that affects \>10% of the general population worldwide, amounting to \>800 million individuals. The diagnosis of CKD is established by laboratory testing, most often by estimating glomerular filtration rate (GFR) from a filtration marker, such as serum creatinine or cystatin C, using various formulas, or by testing urine for albumin or protein (or both). Pentoxifylline (PTX), a synthetic dimethylxanthine derivative used initially to treat intermittent claudication in patients with peripheral arterial disease due to its hemorheological effects, has been shown to have potent antioxidant, anti-inflammatory, antidiabetic, anti-cellular-damage, and antifibrotic effects.

Interventions

DRUGAngiotensin-converting enzyme inhibitors (Ramipril)

Patients received the standard therapy. The routine standard consisted of angiotensin-converting enzyme inhibitors (ACEI) (Ramipril 1.25 mg), a calcium-based phosphate binder (calcium acetate 700 mg, containing 180 mg of calcium), alfacalcidol (0.25 µg), antihypertensive medications, and diuretics.

DRUGPentoxifylline

Patients received one capsule of Pentoxifylline 400 mg twice daily for 6 months, in addition to their standard therapy.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ˃ 18 years old. * Both sexes. * Patients with chronic kidney disease (CKD) stages G3, G4. * Patients with proteinuria \< 1 g.

Exclusion criteria

* Patients who are terminally ill. * Patients with Diabetes mellitus. * Patients with proteinuria \> 1 g. * Patients with a history of hemodialysis. * Patients with active infection or hospitalized. * Patients with recent cerebral and /or retinal Hemorrhage. * Patients taking warfarin or theophylline-containing drugs. * women who are taking oral contraceptives, pregnant, or lactating * Patients with a history of adverse reactions to Pentoxifylline. * Patients with polycystic kidney disease. * Patients with obstructive uropathy.

Design outcomes

Primary

MeasureTime frameDescription
Levels of inflammatory marker3 months post-procedureLevels of inflammatory marker was recorded.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026