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临床试验/NCT05080920
NCT05080920已完成不适用

A Pilot, Randomized, Double Blind, Placebo Controlled Study to Evaluate an Immune System Modulator Nutritional Supplement for the Prevention of Infections in Cancer Patients Receiving Oncologic Treatment During the COVID-19 Pandemia.

Fundación Investigación E Innovación Biomédica Hospital Universitario Infanta Sofia-Henares2 个研究点 分布在 1 个国家目标入组 109 人开始时间: 2020年10月28日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
109
试验地点
2
主要终点
Number of infectious events

研究概览

简要总结

This study is designed to assess the safety and efficacy of Rosmalip® nutritional supplement compared to placebo in subjects with solid cancer for the prevention of infections including COVID-19.

详细描述

Cancer patients undergoing oncologic treatments frequently have comorbidities and suffer immunosuppresion, toxicities and exposure to nosocomial pathogens. As a result, they are at increased risk of infections, including COVID-19. It is of utmost importance to find therapies that can prevent infections with as less toxicity as possible. Rosmalip® is a nutritional supplement developed as a molecular nutrition, composed of a rosemary supercritical extract at concentrations approved by EFSA -with in vitro and in vivo antitumor effects that are independent of its antioxidant and anti-inflammatory properties- in a lipidic vehicle that has shown in preclinical and clinical studies to potentiate innate immunity without apparent toxicity. Being a product of easy synthesis its effects on immunity, inflammation and cancer, could be of interest to prevent and ameliorate infections, including COVID-19.

In this pilot study it is hypothesized that Rosmalip® could help to prevent or ameliorate infections, including COVID-19, in oncologic patients under active treatment. Secondarily, it is also hypothesized to have metabolic beneficial effects.

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with a solid cancer under active Anticancer Treatment (including Chemotherapy, Immunotherapy, Hormone Therapy, Targeted Therapy)
  • Informed consent signature

排除标准

  • Allergies to fish
  • Vitamin, Antioxidants consumers and who would no accept to stop taking them 1 week before and during the study
  • Disphagia
  • Bilirrubin higher than 1.5 Upper Normal Limit (UNL)/ Creatinin > 1.5 UNL
  • Severe organic dysfunction
  • Cardiac dysfunction
  • Cholangitis/ Biliary tract obstruction
  • Immunodeficiency or Immflamatory disease (HIV, Inflammatory Bowel Disease, Collagenosis)
  • Dementia or Psychiatric severe disease
  • Pregnancy or Breastfeeding
  • Previous diseases that interfere lipid carrier absorption

结局指标

主要结局

Number of infectious events

时间窗: 6 months

Number of infectious events according to International Sepsis Forum Consensus

次要结局

  • Evolution of Quality of life(6 months)
  • Changes in C-reactive protein(6 months)
  • Number of SARSCoV2 infections(6 months)
  • Changes in NLR (neutrophils to lymphocytes ratio).(6 months)
  • Changes in ferritin(6 months)
  • Changes in transferrin(6 months)
  • Changes in number of peripheral blood mononuclear cells(6 months)
  • Changes in number of CD4 and CD8 lymphocyte populations(6 months)

研究者

发起方
Fundación Investigación E Innovación Biomédica Hospital Universitario Infanta Sofia-Henares
申办方类型
Other
责任方
Principal Investigator
主要研究者

Enrique Casado Sáenz

Head of Oncology

Fundación Investigación E Innovación Biomédica Hospital Universitario Infanta Sofia-Henares

研究点 (2)

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