跳至主要内容
临床试验/NCT05372289
NCT05372289招募中不适用

Immunonnutrition in Spine Surgery to Improve Patient's Outcome: a Randomized Controlled Trial

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio1 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2022年3月16日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
136
试验地点
1
主要终点
Amelioration of functions evaluated through the Oswestry Disability Index (ODI)

研究概览

简要总结

A malnutritional status is known to be associated with altered immune function, reduced function, and worsen outcomes after orthopedic surgery. Medical and surgical complications are not uncommon in Orthopedics and infection rates are potentially life-threatening complications, with the highest morbidity, mortality, and healthcare costs. Most patients undergoing orthopedic surgery are elderly, malnourished, osteosarcopenic, sedentary, anemic, and suffer from low levels of vitamin D. A mono-nutrient supplement may be not sufficient for supporting the arthrodesis techniques, which are invasive open surgeries procedures with significant blood losses and the need of transfusions. In this therapeutic area, immuno-nutrition has been used in spine surgery, with the reduction of complications, revisions, and readmissions. In addition, prosthetic surgery outcomes have been observed to ameliorate by using this nutritional support. Therefore, preoperative oral immuno-nutrition therapy may be applied in older adults undergoing spine surgery to improve patients' outcomes and reduce complications.

This is a randomized, controlled, open-label, 2-arm non-parallel-group, single-center interventional study to assess the efficacy of an immuno-nutrition therapy vs. hospital standard of care in spine surgery to improve patients' outcomes. This is a single primary endpoint study. A total of 136 patients from IRCCS Orthopedic Institute Galeazzi in Italy will be recruited and assigned in a 1:1 ratio to the treatment arm.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

盲法说明

In this study, the primary endpoint assessors, who are assessing parameters constituting the primary endpoints, will be masked to the treatment regimen. Any personnel involved with the statistical analysis and interpretation of the data and results will be masked to the treatment regimen until database lock.

入排标准

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

入选标准

  • male and female sex, of all ethnicities, aged over 60
  • arthrodesis involving ≥ 6 vertebrae
  • American Society of Anesthesiology (ASA) risk: 1, 2, or 3
  • Absence of neurological or psychiatric disorders
  • Signing of informed consent and consent to collaborate in all study procedures
  • Patients who meet the clinical requirements to undergo their first spinal surgery

排除标准

  • American Society of Anesthesiology (ASA) risk: 4
  • No cervical arthrodesis
  • Diagnosis of neurological or psychiatric disorders
  • Revisions
  • Therapy with other supplements at the time of the first visit 0
  • Known allergy or adverse food reactions
  • Chronic inflammatory or autoimmune diseases (e.g. rheumatoid arthritis)
  • Gastrointestinal disorders
  • Conditions that do not allow to undergo surgery

结局指标

主要结局

Amelioration of functions evaluated through the Oswestry Disability Index (ODI)

时间窗: 3 months

次要结局

未报告次要终点

研究者

发起方
I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
申办方类型
Other
责任方
Sponsor

研究点 (1)

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