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临床试验/CTRI/2024/03/064164
CTRI/2024/03/064164尚未招募Unknown

Effectiveness of L-carnitine on paclitaxel induced myopathy and peripheral neuropathy in breast cancer patients : A randomized, double blind, placebo-controlled trail.

SRM College of Pharmacy1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年3月25日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Serum Creatine kinase MM (CK MM) and

研究概览

简要总结

It was evident that the patient receiving Paclitaxel as a first-line chemo therapeuticagent tend to

develop myopathy on successive chemo-cycle.

This myopathic condition expedite the reduction of quality of life of the patient receiving

paclitaxel.

The patient experience severe muscle fatigue and loss of strength which affects the daily

activityof the patient and increase risk of fall by several folds.

L-carnitine which is an energy sparing over the counter supplement works by producing energy

(ATP) from the reserved fat in the body.

The so-called ATP aids in providing energy and reduce the muscle fatigue.

Ubiquitin proteasome system plays a role in protein breakdown in tissues. L-carnitine act on

this system and prevents protein breakdown thereby prevent muscle loss and myopathy.

L-Carnitine even improves the peripheral neuropathy by decreasing the numbness and pricking

pain. Hence, we have designed an interventional trial to evaluate the effect of L-carnitine on

paclitaxel induced myopathy and peripheral neuropathy in breast cancer patients

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Double

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
Female

入选标准

  • 1.patients with pre-existing myopathy and peripheral neuropathy induced by paclitaxel and those have high risk for developing these are included.
  • 2.patients willing to give informed consent.

排除标准

  • 1.patients with history of ESRD and are excluded.
  • 2.patients with peripheral neuropathy and myopathy precipitated by other disease and drugs are excluded.

结局指标

主要结局

Serum Creatine kinase MM (CK MM) and

时间窗: Baseline and week 26

Nerve conduction study

时间窗: Baseline and week 26

次要结局

未报告次要终点

研究者

发起方
SRM College of Pharmacy
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Duraimavalavan

SRM Medical College Hospital and Research centre,

研究点 (1)

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