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临床试验/NCT02845427
NCT02845427已完成不适用

Closed Suction Drain or Not After Total Hip Arthroplasty: A Randomized Controlled Trial

Assiut University2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2016年2月最近更新:
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
100
试验地点
2
主要终点
change in Hb level

研究概览

简要总结

Comparative randomised study to clarify which better to use or no use of closed suction drain system after total hip arthroplasty regarding amount of blood loss, need for blood transfusion, risk for superficial infection, ecchymosis, wound discharge, effect on early post-operative rehabilitation. Patients will be followed up for one month postoperative clinically (Harris Hip score system), laboratory (Hb level), and radiologically (A-P view plain x-ray of the hip).

详细描述

Total Hip Arthroplasty (THA) wounds are prone to formation of hematomas. Hematomas may increase the incision tension, leading to wound discharge and providing a good medium for bacteria, increase post-operative pain, limitation of range of motion of hip joint and prolong post-operative rehabilitation duration, also may cause ecchymosis, and tension vesicles around the surgical wound.

So use of closed suction drain system may reduce these complications. Nevertheless some recent studies have claimed that drainage can cause other complications and does not reduce hematoma formation and risk for infection. Furthermore, some studies have shown that drainage increase blood loss after THA which may both lead to increase blood transfusion requirements and provide an entry point for skin microorganisms.

Some other studies have found that no significance between use and non use of suction drain after THA.

So the investigators will take this issue for study a comparison between benefits and hazards of use and non use of suction drain after THA.

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
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

  • Primary total hip arthroplasty (THA)

排除标准

  • Revision cases
  • Uncontrolled bleeding tendency (prothrombin conc. Less than 70%)
  • History of deep venous thrombosis
  • Sever liver impairment (liver failure)
  • Sever renal impairment (S. creatinine more than 3)

研究组 & 干预措施

A(drain group)

Active Comparator

patients of primary THA will have closed suction drain introduced intraoperative at surgical site

干预措施: closed suction drain (Device)

B(No drain group)

Placebo Comparator

patients of primary THA will have the surgical wound be closed with no suction drain

干预措施: no suction drain (Procedure)

结局指标

主要结局

change in Hb level

时间窗: preoperative and 24 hrs postoperative

次要结局

  • amount of blood loss(upto 24 hrs postoperative)
  • amount of blood transfusion(upto 24 hrs postoperative)

研究者

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

Yasser E khalifa

professor doctor of orthopedic and traumatology

Assiut University

研究点 (2)

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