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临床试验/NCT07108777
NCT07108777招募中2 期

Clinical Study to Evaluate the Possible Protective Effect of L-Carnitine Against Cisplatin-Induced Nephrotoxicity

Tanta University1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2025年8月10日最近更新:
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
46
试验地点
1
主要终点
change in serum creatinine and creatinine clearance

研究概览

简要总结

The goal of this clinical trial is to assess the possible reno-protective effect of L-carnitine against cisplatin-induced nephrotoxicity in patients receiving cisplatin-based chemotherapy. The main question it aims to answer is:

Does L-carnitine have the ability to protect the kidney against cisplatin-induced nephrotoxicity?

详细描述

Cisplatin is one of the most effective chemotherapeutic agents that has been used for more than 50 years for a different solid Tumers. Nevertheless, its administration is associated with toxicity, including nephrotoxicity which can affects 25-35% of treated patients. Cisplatin nephrotoxicity mainly explained by accumulation in the renal tubules mostly in the proximal and distal tubules where it inhibits and alters the expression pattern of several membrane transporters and water channels and inhibits mitochondrial function and ATP production, thus generating oxidative stress. Cisplatin nephrotoxicity is also associated with an inflammatory response that plays a significant role in this event. Tumor necrosis factor alpha (TNF- α) is a pleiotropic pro-inflammatory cytokine that signals via TNFRSF1A and TNFRSF1B to activate nuclear factor kappa B (NF-κB) or Mitogen-activated protein kinase (MAPK), eventually leading to cytokine production and/or death signaling. L-carnitine owing to its antioxidant and anti-inflammatory properties has been used as a candidate for nephroprotection against drug induced nephrotoxicity (DIN). L-carnitine significantly ameliorates DIN in animal studies especially against cisplatin-induced renal damage. Inhibition of reactive oxygen species generation, lipid peroxidation, matrix remodeling and apoptosis, anti-inflammatory properties and improvement in carnitine deficiency has been suggested as probable nephroprotective mechanisms of L-carnitine.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Care Provider)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female patients.
  • Newly diagnosed patients with cancer and with an indication for cisplatin - based chemotherapy.
  • Age between 18 and 75 years.
  • No serious cardiopulmonary comorbidity which could impair involvement in the study.
  • Creatinine clearance value above 50 mL/min/1.73 m².
  • Patients who will scheduled to receive at least 3 cycles of cisplatin.
  • Patients with no previous renal diseases (including acute nephropathy, acute and chronic renal failure).

排除标准

  • Pregnancy or lactation.
  • Metastasis to the central nervous system.
  • Psychiatric disorders.
  • Prior treatment with platinum derivatives.
  • Hypersensitivity to cisplatin, carboplatin or other platinum derivatives.
  • Patients with active infection or any symptoms of sepsis.
  • Acute renal failure or renal surgery within the last 3 months.
  • Patients unfit for cisplatin (patients with impaired renal function, sensorineural hearing loss and cardiomyopathy).
  • Patients with known history or current treatment with nephrotoxic agents.
  • Taking other antioxidant supplements such as Vitamins C and E.

研究组 & 干预措施

L-carnitine group

Active Comparator

This group will receive the standard chemotherapy protocol (cisplatin -based chemotherapy) plus L-carnitine 350 mg (L-carnitine®) three times daily by oral.

干预措施: L-Carnitine Tartrate (Drug)

Placebo group

Placebo Comparator

This group will receive the standard chemotherapy protocol (cisplatin -based chemotherapy) plus placebo tablets with the same criteria of the intervention drug and the same dose.

干预措施: Placebo (Drug)

结局指标

主要结局

change in serum creatinine and creatinine clearance

时间窗: Baseline (before chemotherapy cycles)

serum creatinine average ranges are 0.7 to 1.2 (mg/dL) for males and 0.5 to 1.0 for females.

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

Fatma Mamdouh Elsayed Eweda

Teaching Assistant

Tanta University

研究点 (1)

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