The purpose of this study is to assess the protection of smallpox preexposure vaccination against infection with mpox in real-world individuals with risk factors for mpox.
A Target Trial Emulation study that tries to emulate the sequential specification of a target trial will be conducted measuring and controlling confounders when there is a common cause of vaccination and outcome event. Participants will be provided with a Quick response (QR) code to access the RedCap study platform, which will guide them to the enrolment process. If the participant accepts and meets all the inclusion and none of the exclusion criteria, they will be directed to a baseline survey to self-collect sociodemographic data and information regarding risk factors, sexual behaviour, vaccination, and exposure to mpox. Newly vaccinated participants will be matched 1:1 to unvaccinated controls. The matching will be performed based on the site of recruitment, and self-reported baseline sexual health and practices. Vaccinated and unvaccinated participants will be matched on variables associated with the probability of infection. Follow-up will include regular surveys every month from the index date (i.e., enrolment date in the unvaccinated group, or vaccination date for the vaccinated group), to collect data on change on risk factors, sexual behaviour in the past month, vaccination status, and exposure to mpox. The participant will be asked to self-report if they develop symptoms suggestive of mpox, and the study platform will direct them to a specific mpox infection survey. For each participant, follow-up will end at the earliest of the following events: mpox infection, voluntary withdraw, or the end of the study period. A health record review will be conducted to corroborate the diagnosis of new cases and to provide validity to the self-report.
Study Type
OBSERVATIONAL
Enrollment
3,125
Vaccination with smallpox and mpox vaccine (Live Modified Vaccinia Virus Ankara)
Hospital Clínico San Borja Arriarán
Santiago, Santiago Metropolitan, Chile
Instituto Conmemorativo Gorgas de Estudios de la Salud (ICGES)
Panama City, Panama
Hospital Regional III Honorio Delgado
Arequipa, Peru
Hospital Nacional Arzobispo Loayza
Lima, Peru
Polymerase chain reaction (PCR)-confirmed mpox infection
Mpox PCR positivity in participants with mpox infection symptoms
Time frame: From 14 days after the index date to twelve months after the index date
Polymerase chain reaction (PCR)-confirmed mpox infection
Mpox PCR positivity in participants with mpox infection symptoms
Time frame: From immediately after the index date to twelve months after the index date
Duration of general symptoms
Time from onset to resolution of general symptoms in participants with PCR-confirmed mpox infection (in days).
Time frame: From 14 days after the index date to twelve months after the index date
Severity of rash
Number of mpox lesions (lesions count)
Time frame: From 14 days after the index date to twelve months after the index date
Duration of skin rash
Time from onset to resolution of skin rash in participants with PCR-confirmed
Time frame: From 14 days after the index date to twelve months after the index date
Medical treatment
Requirement of medical treatment (yes/no)
Time frame: From 14 days after the index date to twelve months after the index date
Hospitalization
Requirement of hospital admission (yes/no)
Time frame: From 14 days after the index date to twelve months after the index date
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Hospital Regional Docente de Trujillo
Trujillo, Peru
Germans Trias i Pujol Hospital
Badalona, Barcelona, Spain
Scarring
Residual scarring after mpox (yes/no)
Time frame: From 14 days after the index date to twelve months after the index date
Safety and tolerability
Description of systemic and skin reactions
Time frame: One month after vaccination