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临床试验/NCT04336332
NCT04336332终止2 期

Randomized Comparison of Combination Azithromycin and Hydroxychloroquine vs. Hydroxychloroquine Alone for the Treatment of Confirmed COVID-19

Rutgers, The State University of New Jersey5 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2020年4月1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
75
试验地点
5
主要终点
Changes in Patients Viral Load

研究概览

简要总结

This is a three-arm randomized trial comparing the efficacy of single agent hydroxychloroquine to the combination of hydroxychloroquine and azithromycin, and to a delayed hydroxychloroquine regimen, which will serve as a contemporaneous Day 1-6 supportive care control, in eliminating detectable SARS-CoV-2 on day 6 following the initiation of treatment in order to determine which regimen is more effective.

详细描述

PRIMARY OBJECTIVE:

I. Determine change in viral load at day 6 compared to baseline between two regimens to treat COVID-19 and a contemporaneous control group.

SECONDARY OBJECTIVES:

I. Time to resolution of symptoms (symptom questionnaire)

II. Change in the fever curve resulting in shorter time to afebrile for 48 hours

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
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

  • Patients with proven SARS-CoV-2 infection by an accepted assay with symptoms consistent with COVID-19
  • Ability to measure and quantify viral load by quantitative PCR
  • Age 18 to 89
  • Ability to swallow oral medications
  • Patients must read, understand and sign IRB approved informed consent

排除标准

  • Pregnancy or women who are breast feeding
  • Two consecutive negative assays for SARS-CoV-2 infection
  • Patients that lack decision-making capacity will not be approached to participate in this study
  • Inability to tolerate oral medications
  • Allergy or prior adverse reaction to either azithromycin or hydroxychloroquine sulfate
  • QTc interval > 470 mSEC
  • History of ongoing ventricular cardiac dysrhythmias of grade 2 as described by NCI CTCAE 5.0 criteria
  • History of serious ventricular arrhythmia (VT or VF > 3 beats in a row)

研究组 & 干预措施

Arm 1: Hydroxychloroquine Sulfate + Azithromycin

Experimental
  • Hydroxychloroquine sulfate 200 mg taken by mouth three (3) times a day for 10 days
  • Azithromycin 500 mg taken by mouth on Day 1, followed by
  • Azithromycin 250 mg taken by mouth once (1) time a day for four (4) days.

干预措施: Hydroxychloroquine Sulfate + Azithromycin (Combination Product)

Arm 1: Hydroxychloroquine Sulfate + Azithromycin

Experimental
  • Hydroxychloroquine sulfate 200 mg taken by mouth three (3) times a day for 10 days
  • Azithromycin 500 mg taken by mouth on Day 1, followed by
  • Azithromycin 250 mg taken by mouth once (1) time a day for four (4) days.

干预措施: Hydroxychloroquine Sulfate (Drug)

Arm 2: Hydroxychloroquine Sulfate alone

Experimental

• Hydroxychloroquine sulfate 200 mg taken by mouth three (3) times a day for 10 days

干预措施: Hydroxychloroquine Sulfate (Drug)

结局指标

主要结局

Changes in Patients Viral Load

时间窗: Baseline and day six

Will be assessed at day six compared to baseline between hydroxychloroquine sulfate alone and hydroxychloroquine sulfate plus azithromycin to treat COVID-19.

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

Sabiha Hussain, MD,MPH

Associate Professor of Medicine

Rutgers, The State University of New Jersey

研究点 (5)

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