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NCT05562323Recruiting

Characterization of Vaccine-induced Responses Against Monkeypox (MoVIHvax) An Observational Prospective Cohort Study

Source: ClinicalTrials.gov · Last updated 7 Jul 2026

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Brief summary (registry, in English)

This observational study has been designed to characterize humoral and cellular immune responses after vaccination against monkeypox (MKP) in HIV positive and negative individuals at high risk of MKP infection during the vaccination campaign in the current monkeypox outbreak.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
27 Sept 2022
Start date
14 Sept 2022
Primary completion date
1 Jul 2026
Lead sponsor
Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia
NCT number
NCT05562323

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 14 Sept 2022 to the primary completion date, 1 Jul 2026
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

AI-kivonat: who the study is looking for

Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults at high risk of monkeypox who are getting the monkeypox vaccine, both with and without HIV. It studies their immune response.

Age
18 years or older
Sex
All sexes can join

Main reasons for not taking part

  • Any medical condition or finding that the investigator thinks could raise risks, interfere with the study or make the data hard to interpret

Read by machine on 9 Nov 2026.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Participant has any medical condition and/or finding that in the investigator opinion might increase participant risks, interfere with the study or impair interpretation of study data.

Who the study is looking for

  • Adult individuals of ≥18 years old.
  • Willing to comply with the requirements of the protocol and available for follow-up for the planned duration of the trial.
  • Has understood the information provided and capable of giving informed consent.

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Germans Trias I Pujol HospitalBadalonaSpainRecruiting
VALLE HEBRÓN HOSPITAL/Centro Salud Internacional y Enfermedades Transmisibles DrassanesBarcelonaSpainNot yet recruiting
BCN CheckpointBarcelonaSpainRecruiting

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.