跳至主要内容
临床试验/NCT04526821
NCT04526821终止2 期

Bovine Lactoferrin for the Prevention of COVID-19 Infection in Physicians and Nurses in Hospitals in Lima, Peru: a Double Blinded Randomized Clinical Trial (LF-COVID)

Universidad Peruana Cayetano Heredia2 个研究点 分布在 1 个国家目标入组 209 人开始时间: 2020年10月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
209
试验地点
2
主要终点
Number of COVID-19 infections during the 12 weeks of intervention

研究概览

简要总结

Clinical trial in health care personnel (physicians, nurses or nurse assistants) to determine the effect of orally-administered bovine lactoferrin to prevent SARS-CoV-2 infection. Participants will be randomized to receive daily bovine lactoferrin plus standard measures during 12 weeks or placebo (maltodextrine) for the prevention of SARS-CoV-2. The target enrollment is 336 participants. Each study participant will be monitored twice a week for symptoms of COVID-19 and if symptoms occur, a RT-PCR will be performed. Additionally, we will evaluate asymptomatic infections, by measuring SARS-CoV-2 serology every 4 weeks.

详细描述

The SARS-CoV-2 infection has affected more than 100 countries around the world being classified as a pandemic by the World Health Organization. Health care providers are at high risk to become infected with the SARS-CoV-2 due to their continuous exposition to infected patients. Multiple strategies are being developed as potential prophylactic regimens, however to date (4th Aug 2020) none has proven to be effective for preventing the SARS-CoV-2 infection. Lactoferrin, an iron-binding protein with multiple physiological functions (anti-microbial, anti-inflammatory, and immunomodulatory), is one of the most important proteins present in mammalian milk. It has shown to inhibit the SARS entry to target cells by inhibiting the union of the SARS-CoV-2 spike protein with its receptor (ACE-II receptors), blocking the heparan sulfate proteoglycan receptor and it decreases the viral load of SARS-CoV-2 infecting culture cells in in vitro models. The study hypothesis is that lactoferrin given as a daily oral food supplement to health care workers will decrease the frequency of SARS-CoV-2 infection. The investigators will conduct a randomized double blinded placebo control clinical trial in physicians, nurses and nurse assistants who work in areas of care for patients with COVID-19 (emergency, hospitalization, and Intensive Care Unit) in hospitals in Lima, Peru, to determine the effect of bovine lactoferrin on the prevention of COVID-19 infection.

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 59 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Man or woman over 18 and under 60 years old
  • Physicians or nurses or nurse assitant who work in areas of care for patients with COVID-19 (emergency, hospitalization, and Intensive Care Unit) in hospitals in Lima, Peru.
  • Healthy participants, without COVID-19 suggestive symptoms
  • Participant who wants to participate and signs the informed consent.

排除标准

  • Participant who had a previous diagnosis of COVID-
  • Participant positive in the initial screening for IgM or IgG or a positive RT-PCR for SARS-CoV-
  • Participant with the following comorbidities: hypertension, coronary heart disease, diabetes mellitus, obesity, chronic lung disease, cancer, kidney failure, or other hematological disease.
  • Pregnant woman.
  • Participant that are part of another clinical trial or are taking any supplement or preventive treatment for COVID-
  • Participant with known allergy to cow's milk protein.

研究组 & 干预措施

Bovine Lactoferrin

Experimental

Bovine Lactoferrin plus standard measures of personal protection.

干预措施: Bovine Lactoferrin (Drug)

Maltodextrin

Placebo Comparator

Maltodextrin plus standard measures of personal protection.

干预措施: Maltodextrin (Dietary Supplement)

结局指标

主要结局

Number of COVID-19 infections during the 12 weeks of intervention

时间窗: Twelve weeks

The primary study outcome will be defined by IgM, IgG and/or RT-PCR positivity for SARS-CoV 2.

次要结局

  • Severity of the COVID-19 infection(Twelve weeks)
  • Duration of symptoms of the COVID-19 infection(Twelve weeks)
  • Frecuency of symptoms of the COVID-19 infection(Twelve weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验