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临床试验/NCT05580965
NCT05580965已完成不适用

The Effect of Duration of Pressure Applied After Blood Sample Collection on the Development of Ecchymosis in Geriatric Patients Using Oral and Subcutaneous Anticoagulants: A Randomized Controlled Trial

Saglik Bilimleri Universitesi2 个研究点 分布在 2 个国家目标入组 164 人开始时间: 2021年10月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
164
试验地点
2
主要终点
number of participants with ecchymosis developed.

研究概览

简要总结

This study aimed to evaluate the effect of different durations of a specific pressure applied after blood collection on the development of ecchymosis in geriatric patients using oral and subcutaneous anticoagulants.

详细描述

The research sample consisted of patients hospitalized in the Geriatrics Clinic of a city hospital. This study aimed to evaluate the effect of different durations of a specific pressure applied after blood collection on the development of ecchymosis in geriatric patients using oral and subcutaneous anticoagulants. In this study, whether ecchymosis developed at the 24th, 48th and 72nd hours after the blood collection procedure was evaluated.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Prevention
盲法
Single (Investigator)

入排标准

年龄范围
65 Years 至 93 Years(Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients aged 65 years and over
  • who voluntarily agreed to participate in the study
  • who used oral (Rivaroxaban 10-15-20 mg, Dabigatran, 75-110-150 mg, Apixaban 2.5-5 mg) and subcutaneous (Enoxaparin sodium 6000-4000 anti-Xa IU/0.6-0.4 ml) anticoagulants
  • who were literate in Turkish
  • who were scheduled for blood collection
  • who would undergo blood collection from the antecubital site with vacutainer

排除标准

  • patients with communication problems
  • patients with hematoma, ecchymosis, and scarring in the antecubital site
  • patients who would be discharged before 72 hours
  • patients with coagulation disorders

结局指标

主要结局

number of participants with ecchymosis developed.

时间窗: at the 72 nd hours

In this study, whether ecchymosis developed at the 24th, 48th, and 72nd hours after the blood collection procedure was evaluated.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Tulay Basak

Professor

Saglik Bilimleri Universitesi

研究点 (2)

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