Skip to content

Monkeypox ASymptomatic Shedding: Evaluation by Self-Sampling MPX-ASSESS

Monkeypox ASymptomatic Shedding: Evaluation by Self-Sampling MPX-ASSESS

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05443867
Acronym
MPX-Assess
Enrollment
27
Registered
2022-07-05
Start date
2022-06-22
Completion date
2022-08-25
Last updated
2023-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Monkey Pox

Brief summary

Monkeypox (MPX) is a viral zoonosis, caused by the Monkeypox virus (MPXV), a DNA virus that belongs to the Orthopoxvirus genus and is closely related to the variola virus, the causative agent of smallpox. Until recently the spread of MPX was mainly confined to the Central African rainforest and to parts of West Africa. However, in May 2022, several cases of MPX were detected throughout Europe and Northern America, albeit with a different presentation than previously seen. Many questions remain on this new presentation of the disease: what the exact mode of transmission is, how contagious the virus really is and whether asymptomatic carriers exist. With this study the researchers aim to perform a close follow-up study of close contacts of MPX confirmed cases. Participants are recruited among high and very high risk contacts of confirmed monkeypox patients that presented to the ITM for diagnosis (index). Contacts that are asymptomatic (for symptoms compatible with MPXV infection according to national case definitions) at the time of recruitment will be enrolled. Contacts of the index case that are symptomatic at recruitment or become symptomatic during follow-up will be invited for sample collection at different timepoints until 21 days after contact as suspect cases.

Interventions

None listed

Sponsors

Institute of Tropical Medicine, Belgium
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Be a high risk or very high-risk contact of a laboratory confirmed monkeypox case, with: * Very high-risk contact: * Sexual partner(s) * Prolonged skin-to-skin contact while the patient had skin lesions * High risk contact * living in the same household or similar environment (e.g. camping, spending the night, etc.); * shared clothing, bedding, utensils, etc., while the patient had skin lesions * healthcare workers with unprotected contact (inadequate or no PPE) 2. Last exposure to the monkeypox index case of less than 21 days ago 3. Adult participants (≥ 18 years old) of any gender 4. Written informed consent is obtained from the participant

Exclusion criteria

1. Presenting with symptoms compatible with MPX: * an unexplained rash on any part of the body AND * one or more of the following symptoms: fever, headache, back pain, fatigue, lymphadenopathy (localised or generalised) 2. Inability or unwillingness to comply with the proposed follow-up schedule

Design outcomes

Primary

MeasureTime frameDescription
Secondary attack rate of MPXV infection in contacts, defined by PCR positivity on any sampleUntil 21 days after contact with index caseSecondary attack rate of MPXV infection in contacts, defined by PCR positivity on any sample

Secondary

MeasureTime frameDescription
Rate of seroconversion in contacts, defined as a positive IgG (immunoglobulineG) for monkeypoxUntil 21 days after contact with index caseTo evaluate the rate of seroconversion in contacts (positive IgG for MPX) within 21 days after contact with index case
Proportion of seroconversion in PCR positive contacts vs PCR negative contacts, defined as negative MPXV PCR in all samples until the end of the follow-up periodUntil 21 days after contact with index caseProportion of seroconversion in PCR positive contacts vs PCR negative contacts, defined as negative MPXV PCR in all samples until the end of the follow-up period
Time to seroconversion overall, in symptomatic and asymptomatic contacts, and in PCR positive and negative casesUntil 21 days after contact with index caseTime to seroconversion overall, in symptomatic and asymptomatic contacts, and in PCR positive and negative cases
Proportion of PCR positive participants with asymptomatic infection at time of first positive PCRUntil 21 days after contact with index caseProportion of PCR positive participants with asymptomatic infection at time of first positive PCR
Proportion of PCR positive participants developing symptoms within the follow-up periodUntil 21 days after contact with index caseProportion of PCR positive participants developing symptoms within the follow-up period
Proportion of asymptomatic infections on number of contacts in follow-up. Asymptomatic infections are defined as contacts with positive MPXV PCR on any clinical sample, without development of any symptoms.within 3 weeks after exposure or within 1 week after PCR positivity, whichever follow-up is longerProportion of asymptomatic infections on number of contacts in follow-up. Asymptomatic infections are defined as contacts with positive MPXV PCR on any clinical sample, without development of any symptoms within 3 weeks after exposure or within 1 week after PCR positivity, whichever follow-up is longer
Time from MPXV PCR positivity in any sample to appearance of any symptom overall and per mode of transmission (close personal contact; anal, vaginal or oral receptive sexual contact; and insertive sexual contact)at the end of the 3-week follow-up periodTime from MPXV PCR positivity in any sample to appearance of any symptom overall and per mode of transmission (close personal contact; anal, vaginal or oral receptive sexual contact; and insertive sexual contact)
Time from MPXV PCR positivity in any sample to appearance of skin lesionsat the end of the 3-week follow-up periodTime from MPXV PCR positivity in any sample to appearance of skin lesions
Time from confirmed exposure to first PCR positivityat the end of the 3-week follow-up periodTime from confirmed exposure to first PCR positivity
Time from confirmed exposure to appearance of skin lesionsat the end of the 3-week follow-up periodTime from confirmed exposure to appearance of skin lesions
Description of the type of symptoms observed in monkeypox contactswithin 3 weeks after last exposureDescription of the type of symptoms observed in monkeypox contacts within 3 weeks after last exposure
Frequency of symptoms observed in monkeypox contactswithin 3 weeks after last exposureFrequency of symptoms observed in monkeypox contacts within 3 weeks after last exposure
Timing of symptoms observed in monkeypox contactswithin 3 weeks after last exposureTiming of symptoms observed in monkeypox contacts within 3 weeks after last exposure
Distribution of skin lesions for sexual contacts versus close personal contacts. (per body surface and per category: local vs generalized skin lesions)at the end of the 3-week follow-up periodDistribution of skin lesions for sexual contacts versus close personal contacts. (per body surface and per category: local vs generalized skin lesions)
Proportion of contacts presenting with systemic symptoms after sexual exposure versus those with close personal contacts exposureat the end of the 3-week follow-up periodProportion of contacts presenting with systemic symptoms after sexual exposure versus those with close personal contacts exposure
Number of contacts with the defined risk and protective factorsAt baselineNumber of contacts with the defined risk and protective factors
Proportion of presence of defined factors in PCR positive contacts.Until the end of the 3-week follow-up periodProportion of presence of defined factors in PCR positive contacts.
Proportion of presence of defined factors in symptomatic PCR positive contactsUntil the end of the 3-week follow-up periodProportion of presence of defined factors in symptomatic PCR positive contacts
Time from confirmed exposure to appearance of any symptomat the end of the 3-week follow-up periodTime from confirmed exposure to appearance of any symptom

Other

MeasureTime frameDescription
Presence of culturable virus in PCR positive samples from pre- or asymptomatic periodUntil the end of the 3-week follow-up periodPresence of culturable virus in PCR positive samples from pre- or asymptomatic period

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026