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临床试验/2022-501132-42-00
2022-501132-42-00已完成4 期

Cohort study of human mpox virus disease

University Of Oxford72 个研究点 分布在 6 个国家目标入组 800 人开始时间: 2022年7月8日最近更新:

试验速览

阶段
4 期
状态
已完成
入组人数
800
试验地点
72
主要终点
Time to lesion(s) resolution, defined a.From a start point of date that positive test is collected (or that treatment started if any delayed treatment) b. Until an endpoint of up to 14 days since inclusion (or since commencement of treatment if any delayed treatment). c.Where lesion resolution is the first day on which all lesions are resorbed, scabbed or desquamated and mucosal ulcers healed. d.And the absence of any serious complications

研究概览

简要总结

To describe clinical outcomes in patients with mpox virus disease treated and not treated with tecovirimat (or other antiviral drugs)

入排标准

年龄范围
0 years 至 65+ years(0-17 Years, 65+ Years, 18-64 Years)
接受健康志愿者

入选标准

  • All patients, with either laboratory confirmed monkeypox virus disease OR Laboratory confirmation pending, but who are being managed as a presumptive case
  • Informed consent provided for participation in the study

排除标准

  • Presumptive cases with subsequent negative test for MPXV
  • Adults lacking capacity due to a previously present impairing condition

结局指标

主要结局

Time to lesion(s) resolution, defined a.From a start point of date that positive test is collected (or that treatment started if any delayed treatment) b. Until an endpoint of up to 14 days since inclusion (or since commencement of treatment if any delayed treatment). c.Where lesion resolution is the first day on which all lesions are resorbed, scabbed or desquamated and mucosal ulcers healed. d.And the absence of any serious complications

Time to lesion(s) resolution, defined a.From a start point of date that positive test is collected (or that treatment started if any delayed treatment) b. Until an endpoint of up to 14 days since inclusion (or since commencement of treatment if any delayed treatment). c.Where lesion resolution is the first day on which all lesions are resorbed, scabbed or desquamated and mucosal ulcers healed. d.And the absence of any serious complications

次要结局

  • Clinical status defined by a) Clinical status on day 14 and day 28 according to an ordinal scale assessed by a physician or a study nurse. The ordinal scale is a) all lesions resolved and no serious complications, b) one or more lesions are active and no serious complications, c) serious complication and/or hospitalization due to mpox, or d) death. b) Evidence of recrudescence or relapse at day 60 and day 180.
  • Virological status defined by: A) Change from baseline in mpox virus DNA levels in throat swabs on days 4, 8, 14 and 28; B)Change from baseline in Monkeypox virus DNA levels in blood on days 4, 8, 14 and 28, C) Presence of Monkeypox virus DNA in lesion swabs on days 4, 8, 14 and 28.
  • In cohort receiving tecovirimat (or other antivirals): Number and type of Serious Adverse Events (SAEs), Suspected Adverse Reactions (SARS) and Suspected Unexpected Serious Adverse Reactions, (SUSARs) within 28 days of enrolment
  • Outcome of pregnancy in women who are pregnant

研究者

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

ISARIC general enquiries

Scientific

University Of Oxford

研究点 (72)

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