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临床试验/IRCT201402233449N16
IRCT201402233449N16已完成2 期

Comparing efficacy of pentoxifyllin ointment and placebo in treatment of bedsore in patients hospitalized in intensive care unit

Vice Chancellor for Research, Tehran University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
100

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

年龄范围
18 years 至 65 years(—)
性别
All

入选标准

  • Inclusion Criteria: Critically ill patients with grade 1 or 2 of bedsore, who will be hospitalized in Intensive Care Unit (ICU) for at-least 14 days and without history of pentoxifyllin hypersensitivity.

排除标准

  • Patients with severe bedsore requiring antibiotic therapy and worsening of bedsore during treatment course will be excluded from the study.

研究者

发起方
Vice Chancellor for Research, Tehran University of Medical Sciences

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