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临床试验/NCT04486144
NCT04486144已完成不适用

Impact of a Proprietary Extract of Nerium Oleander on Immune Function as Evidenced by Clinical Symptoms and Mortality :A Feasibility Study

HealthQuilt2 个研究点 分布在 1 个国家目标入组 82 人开始时间: 2020年5月20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
HealthQuilt
入组人数
82
试验地点
2
主要终点
COVID19 symptoms

研究概览

简要总结

Assess the impact of a proprietary extract of Nerium oleander on immune function as evidenced by COVID-19 symptoms and mortality in COVID-19 positive patients and their close contacts compared to controls that did not receive the extract.

详细描述

This is an exploratory study based on positive in-vitro, and in-vivo (humans) that appear to support an immune function benefit. Up to 100 patients that are COVID-19 positive in the ambulatory setting will be invited to participate. After informed consent is obtained, patients will be in either the Intervention Group (receive extract) or Comparison Group (did not receive extract). A baseline assessment and record review will be conducted to assure eligibility criteria. Patients in the Intervention Group will be given .5 ml (6.25 mg of extract) every 6 hours for 5 days, total of 25 mg per day / 125 mg for 5 days. Patient vital signs (temperature, pulse oximetry, blood pressure) and CDC symptoms / side effects will also be tracked. A dedicated medical oversight team with 24 / 7 access to care will be provided to monitor safety and tolerance. Patients will be followed for 10 days. Baseline antibody, RT-PCR, and live virus will be collected on Day 1, Day 5, and Day 10. A Data Monitoring Committee at the Schull Institute will meet weekly to review data.

研究设计

研究类型
Interventional
分配方式
Non 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

  • COVID 19 positive or close contact of COVID 19 positive
  • No use of cardiac glycosides or other antiarrhythmic medications

排除标准

  • No use of cardiac glycosides or other antiarrhythmic medications
  • No allergy to coconut oil

结局指标

主要结局

COVID19 symptoms

时间窗: Every 6 hours for 10 days

The CDC list of symptoms and "other".

Mortality

时间窗: 10 days from enrollment into the Study, e.g. Day 10

A patient in any arm that dies.

次要结局

  • RT-PCR COVID19 Test(Day 1, Day 5, Day 10)
  • COVID19 Live Virus(Day 1, Day 5, Day 10)

研究者

发起方
HealthQuilt
申办方类型
Other
责任方
Sponsor

研究点 (2)

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