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临床试验/NCT03821597
NCT03821597已完成不适用

The Effect of Intraoperative Sequential Compression Devices on Fibrinolysis in Plastic Surgery Outpatients: A Randomized Trial

Swanson Center2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2018年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
Change in plasma levels of tissue plasminogen activator and plasminogen activator inhibitor-1

研究概览

简要总结

This study investigates a possible fibrinolytic effect of sequential compression devices (SCDs). These devices have been used for decades to reduce risk of deep venous thrombosis (DVT). However, a randomized study in plastic surgery outpatients has not been done. This study is undertaken to remedy that deficiency in our knowledge base.

详细描述

Protocol: The Effect of Intraoperative Sequential Compression Devices on Fibrinolysis in Plastic Surgery Outpatients

  1. Study Synopsis

Deep venous thrombosis (DVT) is a serious and potentially life-threatening surgical complication. Sequential compression devices (SCDs), also called intermittent pneumatic compression, are widely used by surgeons in an effort to reduce risk. In addition to a possible mechanical effect, some investigators believe that these devices reduce the coagulability of blood by altering the fibrinolytic balance. This investigation is meant to evaluate any possible effect of these devices on fibrinolytic activity.

The SCDs are not being investigated for a new indication. This study is meant to determine whether these commonly used devices have any effect on blood coagulability. This study is not intended to determine whether SCDs affect DVT rates. 2. Background

The investigator (ES) has conducted a literature search on this topic. There is no published prospective randomized study available investigating a possible fibrinolytic effect of SCDs in surgical patients. Therefore any clinical benefit remains speculative. 3. Objective

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • All healthy patients aged 18 or more.

排除标准

  • These conditions include suspected active or untreated DVT, pulmonary edema, congestive heart failure, thrombophlebitis or an active infection, vein ligation, gangrene, dermatitis, open wounds, a recent skin graft, massive edema or extreme deformity of the leg, neuropathy, legs that are insensitive to pain, or when increased venous or lymphatic return is undesirable.

研究组 & 干预措施

Sequential compression devices

Experimental

Sequential compression devices (SCDs) are applied during surgery.

干预措施: Sequential compression devices (SCDs) (Procedure)

No sequential compression devices

Active Comparator

No sequential compression devices are applied.

干预措施: No sequential compression. (Procedure)

结局指标

主要结局

Change in plasma levels of tissue plasminogen activator and plasminogen activator inhibitor-1

时间窗: 1-2 months

Laboratory testing of serum levels

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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