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临床试验/ACTRN12610000762055
ACTRN12610000762055终止2 期

A Single Site, Randomized, Single-Blind, Parallel-group, Placebo-Controlled Study to investigate reduction of inflammation using Intravenous Sodium Ascorbate in patients with Cellulitis

Biological Therapies0 个研究点目标入组 140 人开始时间: 2010年9月14日最近更新:
适应症

试验速览

阶段
2 期
状态
终止
入组人数
140

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • •Patients will be eligible for the study: 1. Age 18 or over. 2. Cellulitis deemed on grounds of severity to require admission for intravenous antibiotics. 3. Capable of understanding and willing to give written informed consent.

排除标准

  • •The following will exclude patients from randomisation: 1. Dementia or mental state preventing informed consent 2. Refusal to give informed consent 3. Chronic heart failure requiring fluid restriction < 1000ml 4. Acute oliguric renal failure 5. Pulmonary oedema 6. Supplemental ingestion of Vitamin C 7. Known Glucose-6-phosphate dehydrogenase (G6PD) deficiency 8. Any pregnant patients will be excluded (urine pregnancy test to be performed as per hospital protocol prior to randomisation. Negative result must be documented prior to randomisation).9. Patients taking any prohibited medication. 10. Diabetic patients currently on insulin.

研究者

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