跳至主要内容
临床试验/CTRI/2010/091/002947
CTRI/2010/091/002947已完成3 期

A randomized comparative study evaluating the efficacy and tolerability of a 1000 IU/ml topical solution of heparin sodium as compared to a 200 IU/G heparin sodium gel in the management of post infusion superficial thrombophlebitis.

Troikaa Pharmaceuticals Ltd0 个研究点目标入组 200 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • a)Patients in the age group of 18-60 years
  • b)Patients of both sexes
  • c)Patients on IV infusion
  • d)Superficial thrombophlebitis Grade 2-4

排除标准

  • a)Patients below 18 years and above 60 years of age
  • b)Patients on anticoagulants
  • c)Pregnant and lactating women
  • d)Patients with any contraindication to heparin
  • e)Mentally retarded patients
  • f)Unwilling patients
  • g)Patients with known hypersensitivity to any component of the formulation
  • h)Patients with grade 1 or 5 phlebitis
  • i)Application of other topical anti-inflammatory agent.

研究者

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