Viral Clearance and Epidemiological Characteristics in Patients With Monkeypox
NCT ID: NCT05476744
Last Updated: 2023-09-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
77 participants
OBSERVATIONAL
2022-06-28
2023-03-30
Brief Summary
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Detailed Description
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Monkeypox is known to be transmitted by close contact with skin lesions of infected individuals and/or via droplets. It is known that the virus can be detected from skin lesions, in blood, in throat swabs and on occasion urine samples. There is limited information as to whether the virus can be detected or persist in other sites including semen. Serial virological monitoring has been conducted in a small number of individuals and demonstrates that prolonged shedding for at least 2-3 weeks appears to be relatively common. To help control the current outbreak health authorities have used a number of strategies including identifying and isolating cases of monkeypox combined with contact tracing and limited use of ring-vaccination strategies. Because the number of cases seen outside of endemic areas has previously been limited, there is inadequate data to guide decision-making about the duration of isolation, but this is critical to the management of the current outbreak.
The present observational study has been designed to understand the dynamics of viral clearance amongst patients with confirmed monkeypox, by quantifying monkeypox viral load in different specimens trough time, to better inform decision-making about patient management and isolation guidelines. Also, an immune analysis will be performed in a subset of individuals to describe humoral and cellular responses to monkeypox.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Examined by a specialist in sexually transmitted infections (STIs) and found to have lesions suggestive of monkeypox.
3. Symptomatic with symptoms onset date ≤10 days prior to screening/baseline visit.
4. Willing to comply with the requirements of the protocol and available for follow-up for the planned duration of the trial.
5. Has understood the information provided and capable of giving informed consent.
Exclusion Criteria
2. Inability to consent and/or comply with trial protocol
3. An alternative confirmed diagnosis that can fully explain the illness
18 Years
ALL
No
Sponsors
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IrsiCaixa
OTHER
CEEISCAT
UNKNOWN
Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia
OTHER
Responsible Party
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Oriol Mitja
Associate Professor, Infectious Diseases and Global Heaelth
Locations
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Hospital Universitari Germans Trias i Pujol
Badalona, Barcelona, Spain
Atenció Primària Metropolitana Nord
Sabadell, Barcelona, Spain
Drassanes Vall d'Hebron Centre for International Health and Infectious diseases
Barcelona, , Spain
BCN Checkpoint
Barcelona, , Spain
Hospital Universitario 12 de Octubre
Madrid, , Spain
Countries
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Other Identifiers
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MoViE Study
Identifier Type: -
Identifier Source: org_study_id
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