跳至主要内容
临床试验/NCT02255318
NCT02255318Unknown不适用

Primary Prevention of Infections Related to Chambers Implantable Catheter by a Taurolodine Lock in Patients With Cancer Receiving Parenteral Nutrition

Hospices Civils de Lyon3 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2015年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
70
试验地点
3
主要终点
The incidence rate of infections related to chamber implantable catheters (IRCIC) in patients who received Taurolock® versus those who received the usual procedure of saline flush.

研究概览

简要总结

The therapeutic management of patients with cancer often requires the establishment of a chamber implantable catheter. Infections are the main complication of these catheters. These infections may be responsible for a significant impairment of quality of life for patients, and may increase the frequency and duration of hospitalizations. The rate of mortality from these infections is about 17%. The objective of this study is to evaluate the efficacy of a 1.35% taurolidine lock / 4% citrate (TauroLock®) in the primary prevention of infections related to chambers implantable catheter (IRCIC) in cancer patients receiving parenteral nutrition.

This is a, randomized, double-blind clinical trial comparing the incidence of IRCIC in patients receiving Taurolidine lock or concession the usual procedure of rinsing with saline (placebo) (pulsed rinsing with 20 mL of serum physiological and clamping catheter positive pressure). The lock will be instilled after the end of the session IV treatment (chemotherapy, parenteral nutrition, transfusion) before closing the catheter. The primary endpoint will be the rate IRCIC in both groups.

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
Triple (Participant, Care Provider, Investigator)

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

  • Patients aged 18 years and over
  • Patients with solid cancer
  • Patients with implantable catheter
  • Patients receiving parenteral nutrition
  • Patient affiliated to a social security scheme or beneficiary of such a regime

排除标准

  • Patients refusing to participate in the protocol
  • Patients already receiving preventive lock of IRCIC
  • Known citrate or (cyclo) allergy -taurolidine
  • Patients taking other drugs with known contraindications against the citrate or cyclotaurolidine.
  • Participation in another protocol for the prevention of infections associated with central venous catheters
  • Patients who did not sign the consent
  • Patient with a status of socio-legal protection

研究组 & 干预措施

Taurolock

Experimental

Patients received Taurolock lock for 3 months administration.

干预措施: Taurolock (Device)

Placebo

Placebo Comparator

Patients received placebo lock (physiological serum) for 3 months administration.

干预措施: Placebo (Drug)

结局指标

主要结局

The incidence rate of infections related to chamber implantable catheters (IRCIC) in patients who received Taurolock® versus those who received the usual procedure of saline flush.

时间窗: The incidence will be assessed between the inclusion and 3 months after the beginning of the study.

Definition of IRCIC This definition of infections related to chamber implantable catheters will be used for all patients. It is based on the identification of the same germ blood cultures of peripheral vein and those of the central venous line with a differential time greater than 120 minutes growth.

次要结局

  • Duration of hospitalizations for IRCIC.(between the inclusion and 3 months after the beginning of the study)
  • Delay onset of IRCIC(between the inclusion and 3 months after the beginning of the study)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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