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临床试验/NCT07315139
NCT07315139已完成不适用

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

Ain Shams University1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2023年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
1
主要终点
Levels of inflammatory marker

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • 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.

研究组 & 干预措施

Group 1

Active Comparator

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.

干预措施: Angiotensin-converting enzyme inhibitors (Ramipril) (Drug)

Group 2

Experimental

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

干预措施: Pentoxifylline (Drug)

结局指标

主要结局

Levels of inflammatory marker

时间窗: 3 months post-procedure

Levels of inflammatory marker was recorded.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ashraf Hassan

Assistant Professor of Internal Medicine and Nephrology, Faculty of Medicine, Ain shams University, Cairo, Egypt.

Ain Shams University

研究点 (1)

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