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临床试验/NCT05465798
NCT05465798尚未招募2 期

Beta-glucans as Immune Modulators Amongst Hospitalised Patients With COVID-19: A Pilot Randomised Trial

Wohlstand Pharmaceutical1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Symptom duration

研究概览

简要总结

This randomised trial aims to assess the role of beta1-3 glucan supplementation in improving clinical symptoms and other outcomes amongst hospitalised patients with COVID-19.

详细描述

COVID-19 can present as a life-threatening disease characterised by respiratory failure and high circulating levels of inflammatory cytokines. Beta-glucans comprise a heterogeneous group of natural polysaccharides consisting of D-glucose monomers linked by a beta-glycosidic bond. They represent key structural elements of the cell wall and may serve as energy storage in bacteria, fungi including yeast, algae, and plants. In this triple-masked randomised trial, hospitalised patients requiring treatment with supplemental oxygen because of a laboratory-confirmed infection by SARS-CoV-2 will receive supplementation with 1-3 beta-glucans or placebo as part of their standard treatment. The primary endpoint of this trial is the intensity of clinical symptoms as detected by the Wisconsin Upper Respiratory Symptom Survey (WURSS).

Patients requiring mechanical ventilation at baseline will be excluded, as will those with cognitive impairment that precludes the use of clinical assessment scales, patients in which an order to limit therapeutic efforts has been issued, pregnant or breastfeeding women and those who decline to participate in this study. Secondary outcomes will include clinical deterioration requiring admission to an intensive care unit, requirement of high-flow nasal cannula or invasive mechanical ventilation and overall survival. Patients will be followed-up until hospital discharge or up to fifteen days after randomisation. Statistical analyses will be undertaken by a statistician unaware of treatment allocation under the intention-to-treat principle.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • Adult participants with an infection caused by SARS-CoV-2 confirmed with a reverse-transcription polymerase chain reaction (RT-PCR) obtained from a nasopharyngeal swab.

排除标准

  • Life expectancy < 6 months
  • Currently receiving invasive mechanical ventilation at baseline.
  • Cognitive impairment that precludes the use of WURSS or understanding the informed consent form.
  • Refusal to participate.

研究组 & 干预措施

Beta-Glucans

Experimental

Patients allocated to this arm will receive MC 3x3, an oral supplement containing 25mg of 1,3 beta-Glucans daily for up to three consecutive days.

干预措施: MC 3x3 (Drug)

Placebo

Placebo Comparator

Participants allocated to this arm will receive a placebo that will be identical in form to the MC 3x3 pills used the interventional arm. These doses will be scheduled daily and administered orally for up to three consecutive days.

干预措施: Placebo (Drug)

结局指标

主要结局

Symptom duration

时间窗: Up to 2 weeks after randomisation or hospital discharge

Total time with disease manifestations attributable to COVID-19.

Clinical recovery

时间窗: Seven days after randomisation or up to hospital discharge

Number of patients without clinical complaints attributable to COVID-19

Symptom severity

时间窗: WURSS-21 scores calculated 7 days after randomisation

Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.

次要结局

  • C-Reactive protein levels(This laboratory exam will be measured on days 1, 3, 5 and 7 after randomisation.)
  • Invasive mechanical ventilation(Up to seven days after randomisation)
  • Hospital Stay(Until hospital discharge)
  • Neutrophil to lymphocyte ratio(This laboratory exam will be measured on days 1, 3, 5 and 7 after randomisation.)
  • Survival(Up to seven days after randomisation)
  • Absolute lymphocyte count(This laboratory exam will be measured on days 1, 3, 5 and 7 after randomisation.)
  • Intensive Care Unit Admission(Up to seven days after randomisation)

研究者

发起方
Wohlstand Pharmaceutical
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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