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临床试验/NCT04489628
NCT04489628撤回1 期

Tele-health Enabled Clinical Trial for COVID-19: Vitamin D as an Immunomodulator to Prevent Complications and Reduce Resource Utilization in Outpatients

University Hospitals Cleveland Medical Center1 个研究点 分布在 1 个国家开始时间: 2020年8月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
撤回
试验地点
1
主要终点
Patients requiring admission to the hospital or experiencing death

研究概览

简要总结

To determine the efficacy of high dose Vitamin D (an over-the-counter nutritional supplement) in preventing immune-related complications in outpatients with confirmed SARS-CoV-2 infection.

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
Triple (Participant, Care Provider, Investigator)

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

  • ≥ 18 years of age
  • Laboratory confirmed SARS-CoV-2 infection < 4 days before randomization
  • Report of symptoms consistent with SARS-CoV-2 infection (including but not limited to fever, cough, muscle aches, joint pain, change in taste, change in smell, or shortness of breath) <4 days before admission
  • Asymptomatic or mild symptoms (not requiring hospital admission)
  • Access to and ability to use a mobile phone with telehealth capability

排除标准

  • Unable to provide informed consent or comply with study directions
  • Admitted to an acute care bed
  • Baseline serum calcium < 8.8 mg/dL or > 10.2 mg/dl (as evaluated by labs taken in the ER/urgent care)
  • Women who are currently breastfeeding
  • History of kidney stone in the past year or h/o multiple (>1) previous kidney stones
  • Does not have a smart phone that can download apps from Google Play or App Store.
  • No way to keep the phone charged consistently
  • The smartphone is shared with another individual.
  • Required laboratory data is unavailable (eg calcium levels)
  • No new oxygen requirement (see remote monitoring document)
  • Pregnant and lactating mothers.
  • Vitamin D level of 80ng/ml and above
  • No lab work for calcium or vitamin D completed in ED

研究组 & 干预措施

Vitamin D

Active Comparator

Participants will be given 8 capsules of either cholecalciferol 50,000 IU or placebo at study randomization. Participants will be instructed to take 4 capsules on receipt of the treatment package(Day 0), 2 capsules on Day 5, 1 capsule on Day 10, and 1 capsule on Day 15. A phone or text reminder will be included at Days 5, 10, and 15 to take the additional doses of vitamin D.

干预措施: Vitamin D3 or Placebo (Drug)

Vitamin D

Active Comparator

Participants will be given 8 capsules of either cholecalciferol 50,000 IU or placebo at study randomization. Participants will be instructed to take 4 capsules on receipt of the treatment package(Day 0), 2 capsules on Day 5, 1 capsule on Day 10, and 1 capsule on Day 15. A phone or text reminder will be included at Days 5, 10, and 15 to take the additional doses of vitamin D.

干预措施: Doctella telehealth monitoring (Device)

Placebo

Placebo Comparator

Participants will be given 8 capsules of either cholecalciferol 50,000 IU or placebo at study randomization. Participants will be instructed to take 4 capsules on receipt of the treatment package(Day 0), 2 capsules on Day 5, 1 capsule on Day 10, and 1 capsule on Day 15. A phone or text reminder will be included at Days 5, 10, and 15 to take the additional doses of vitamin D.

干预措施: Doctella telehealth monitoring (Device)

结局指标

主要结局

Patients requiring admission to the hospital or experiencing death

时间窗: Days 1 to 15

Proportion of patients requiring admission to the hospital or experiencing death by Day 15

次要结局

未报告次要终点

研究者

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

Dr. Kevin Cooper

Principal Investigator

University Hospitals Cleveland Medical Center

研究点 (1)

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