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临床试验/NCT00137579
NCT00137579已完成4 期

Phase IV, Simple Blind, 2-Parallel Groups Randomized Trial to Evaluate the Safety and Effectiveness of the Intramuscular Vs Subcutaneous Route for the Administration of the Anti-Flu Vaccine in Patients Receiving Oral Anticoagulation

Catalan Institute of Health4 个研究点 分布在 1 个国家目标入组 216 人开始时间: 2003年9月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
216
试验地点
4
主要终点
local pain (scores greater than 3 in the analogic visual scale of pain)

研究概览

简要总结

Until now, the best administration route of the anti-flu vaccine for patients receiving long term oral anticoagulation therapy has been the subcutaneous one; the intramuscular route has not been recommended because it may increase the risk of muscular haematoma. Although this practice is widely extended, no significant differences between the safety of both routes have been found. Some authors, analysing a small group of patients, affirm that the anti-flu vaccine can be administered safely by the intramuscular route on patients receiving long term oral anticoagulation therapy, while a previous opinion article recommended the subcutaneous route without any scientific evidence. Due to this, the investigators have done a clinical trial with the aim of determining the safety and effectiveness of the flu-vaccine intramuscular route in patients receiving long term oral anticoagulation therapy and also to analyse the possible interactions between the vaccine and the oral anticoagulant treatment.

详细描述

Phase IV, simple blind, 2-parallel groups, multicentric randomized trial where each patient will receive a single dose of the recommended by the WHO anti-flu vaccine for the 2003-2004 period, the control group will receive it subcutaneous and intervention group intramuscular. The assignation to each group will be randomized. The study included 4 basic areas of Barcelona city. Three visits have been scheduled for each patient: moment 0, 24 hours and 10 days after the vaccination, and a 7 month follow up period to control the incidence of the flu.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single

入排标准

年龄范围
18 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with oral anticoagulation therapy
  • •Patients who agree to be vaccinated
  • •Patients who agree to participate in the study
  • •Patients older than 18

排除标准

  • •Allergy or hypersensibility to egg, chicken proteins, any component of the vaccine (neomycin, octoxinol-9 or formaldehyd)
  • •INR greater than 4 in the past 2 months
  • •Previous major bleeding
  • •Patients with dementia or with legal tutoring

结局指标

主要结局

local pain (scores greater than 3 in the analogic visual scale of pain)

microbiologically diagnosed flu (yes/no)

International Normalized Ratio (INR) to check the interaction between the vaccine and the oral anticoagulation therapy

次要结局

  • increase of the arm perimeter greater than 1 cm
  • local elemental skin lesions

研究者

发起方
Catalan Institute of Health
申办方类型
Other Gov

研究点 (4)

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