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临床试验/NCT04907877
NCT04907877已完成不适用

Role of Nutritional Support With Probiotics in Adult Outpatients With Symptomatic COVID-19: a Randomized Dietary Study

Nordic Biotic Sp. z o.o.3 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2021年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
70
试验地点
3
主要终点
Global symptom score

研究概览

简要总结

There is evidence that some types of probiotics play a role in alleviation of symptoms of acute respiratory tract infections and bursting immune response to respiratory and enteric viruses. Available data serves a rationale for the study exploring a role of nutritional support with probiotics in adult outpatients with COVID-19. Hypothesis of the study is that a proposed mixture of lactobacilli and bifidobacteria facilitate faster recovery from COVID-19 and enhance specific immune response to SARS-CoV-2 antigens.

详细描述

One hundred adults with confirmed (PCR or antigen test) symptomatic COVID-19 lasting upto 5 days will be screened for the study. When the subject meets enrollment criteria, he/she will be randomized to take an investigational product (probiotic, test dietary supplement, TDS), a mixture of lactobacilli and bifidobacteria or placebo 1 time a day before breakfast for 28 days after enrollment. During observation, the patient will keep Respiratory Illness Diary. Blood serum will be collected at baseline, day 0-5 (Nurse Visit 1), after 28-35 days (Nurse visit 2), and 6 months (Nurse visit 3) for evaluation of anti-SARS-CoV-2 antibodies to nucleocapsid and spike antigents. In 3 months, investigator/family physician will collect Post-COVID-19 Questionnaire

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

入选标准

  • •Age ≥ 18 - ≤ 65 years;
  • •Male or non-pregnant female;
  • •Informed virtual pre-consent and paper signed consent forms;
  • •Confirmed symptomatic COVID-19 lasting 0-5 days;
  • •Subject understands and agrees to comply with study procedures including triple blood analysis for anti-SARS-CoV-2 IgG;

排除标准

  • •Risk for the complicated course of COVID-19 due to:
  • •Hypertension; 1.
  • •Diabetes mellitus; 1.
  • •Immunosuppressive conditions; 1.
  • •Chronic pathology of the respiratory system ; 1.
  • •Chronic pathology of the cardiovascular system ; 1.
  • •Malignant tumor ; 1.
  • •Systemic inflammatory connective tissue disease ; 1.
  • •Cerebrovascular disease ; 1.
  • •Chronic hepatitis. Hepatic cirrhosis; 1.
  • •Inflammatory bowel diseases ; 1.
  • •Chronic kidney disease ;
  • •Drug or alcohol abuse as suspected by investigator;
  • •History of persistent diarrhea of any cause;
  • •Use of pre- or probiotics during the last 2 weeks before enrollment;
  • •Allergy to any components of the TDS;
  • •Technical difficulties to perform virtual study visits.
  • •Inability to perform a blood test for antibodies after 6 months
  • •Inability to swallow capsules, or choking / coughing while eating

研究组 & 干预措施

Placebo

Placebo Comparator

Maltodextrine administered once a day for 28 days

干预措施: Placebo (Dietary Supplement)

Probiotic

Experimental

NordBiotic ImmunoVir, a mixute of bidido- and lactobacteria administered in a dose of 5 billion once a day for 28 days

干预措施: Probiotic (Dietary Supplement)

结局指标

主要结局

Global symptom score

时间窗: 10 days

Clinical score of Coronavirus disease-19; minimal score 0 (healthy), maximal score 36 (worst disease)

次要结局

  • Hospitalization rate(28 days)
  • 8 - point ordinal severity scale of coronavirus disease-19(28 days)
  • Time to recovery(28 days)
  • Percent of completely recovered patients(28 days)

研究者

申办方类型
Industry
责任方
Principal Investigator
主要研究者

Sergei Gerasymov, MD, PhD

Principal Investigator

Nordic Biotic Sp. z o.o.

研究点 (3)

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