Viral Clearance and Epidemiological Characteristics in Patients With Monkeypox

NCT ID: NCT05476744

Last Updated: 2023-09-18

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

77 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-06-28

Study Completion Date

2023-03-30

Brief Summary

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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.

Detailed Description

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Starting in early May 2022 a large number of cases of Monkeypox have been reported in non-endemic countries. Although initial cases appeared to be linked to travel, the majority of subsequent cases appear to have no travel associated risk factors and these cases have predominantly occurred amongst Men who have Sex with Men (MSM) suggesting autochthonous transmission associated with sexual networks.

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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Monkeypox

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

1. Adult male or female individuals of ≥18 years old.
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

1. Severe disease - defined as requires admission to hospital
2. Inability to consent and/or comply with trial protocol
3. An alternative confirmed diagnosis that can fully explain the illness
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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IrsiCaixa

OTHER

Sponsor Role collaborator

CEEISCAT

UNKNOWN

Sponsor Role collaborator

Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia

OTHER

Sponsor Role lead

Responsible Party

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Oriol Mitja

Associate Professor, Infectious Diseases and Global Heaelth

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hospital Universitari Germans Trias i Pujol

Badalona, Barcelona, Spain

Site Status

Atenció Primària Metropolitana Nord

Sabadell, Barcelona, Spain

Site Status

Drassanes Vall d'Hebron Centre for International Health and Infectious diseases

Barcelona, , Spain

Site Status

BCN Checkpoint

Barcelona, , Spain

Site Status

Hospital Universitario 12 de Octubre

Madrid, , Spain

Site Status

Countries

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Spain

Other Identifiers

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MoViE Study

Identifier Type: -

Identifier Source: org_study_id

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