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临床试验/NCT01518335
NCT01518335已完成不适用

A Double-Blind, Randomized, Placebo Controlled Study Evaluating the Use of Platelet Rich Plasma Therapy for Acute Ankle Sprains in the Emergency Department.

Albert Einstein Healthcare Network2 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2009年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
38
试验地点
2
主要终点
Change from baseline of LEFS score, a previous validated 80-point scale used to quantify lower extremity function.

研究概览

简要总结

This research study hopes to determine whether or not platelet rich plasma therapy improves healing time of moderate to severe ankle sprain in comparison to standard of care therapy.

详细描述

The intention of this research project is to study a new treatment for severe ankle sprains.This new treatment is called Platelet Rich Plasma (PRP) therapy and involves injecting concentrated platelet's from a patient's own blood into the site of injury to aid healing. Platelets, aside from their clotting capabilities also serve a role in re-vascularization of tissue as well as collagen repair. PRP therapy has been used in sports medicine for treatment of chronic injuries but has yet to be proven effective in acute injury of a joint. The investigators are comparing treatment and placebo groups based on a subjective patient questionnaire and pain score administered on the day of injury and 2-3 days and 8-10 days follow up.

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
Double (Participant, Care Provider)

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

  • severe ankle sprain
  • X-ray completed

排除标准

  • Pregnancy/breastfeeding
  • Police custody
  • active infection
  • metastatic disease/tumors
  • History of thrombocytopenia
  • Allergy to ester or amine anesthetics
  • On anticoagulant medication
  • Peripheral vascular disease
  • Known coagulopathy

结局指标

主要结局

Change from baseline of LEFS score, a previous validated 80-point scale used to quantify lower extremity function.

时间窗: Day 0; Day2-3; Day 8-10; Day30

The primary outcome of this investigation is change from baseline in LEFS score, a previous validated 80-point scale used to quantify lower extremity function. A difference of 9 points is considered clinically significant.

次要结局

  • Change in pain from baseline(Day 0; Day 2-3, Day 8-10, Day 30)

研究者

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

James Gardner, MD

MD

Albert Einstein Healthcare Network

研究点 (2)

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