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Collection of various sample types from patients with rare/emerging or exotic viruses and Rickettsia for molecular and serological diagnostic test development and validation purposes.

Collection of various sample types from patients with rare/emerging or exotic viruses and Rickettsia for molecular and serological diagnostic test development and validation purposes. - iMONSTER

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON54440
Enrollment
100
Registered
2021-03-02
Start date
2021-03-01
Completion date
Unknown
Last updated
2024-09-23

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

Conditions

Rickettsial infection exotic and/or emerging arboviral and other infection rare and exotic diseases from which some are transmitted by mosquito and other insects

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: *adult and fully capable person *written informed consent provided *strong clinical suspicion by infectious disease clinical specialists of infection with rare/emerging or exotic viruses or Rickettsiae spp based on signs and symptoms in combination with relevant travel history and/or activities presenting at any departments or out-patient clinic of the EMC or confirmed positive external patients/participants (Figure 1, Appendix 1 and 2). Patients will be approached and included by infectious disease clinical specialists, by their treating physician or through municipal public health services or recruited via advertisement.

Exclusion criteria

Exclusion criteria: *written Informed consent NOT provided *

Design outcomes

Primary

MeasureTime frame
Primary end point: creation of a sample pool for diagnostic test development and validation of rare/emerging or exotic viruses and Rickettsia.

Secondary

MeasureTime frame
Secondary end points: 1, to gain knowledge about the kinetics of viral infections and Rickettsiae spp infection; 2. to test the suitability of body fluids and eschar swab for diagnostic use; 3. concordance between PCR test results, virus isolation and (neutralizing) antibody (IgM, IgG) responses; 4. presence and persistence of other markers (e.g. IgM, IgG, IgA, IgE).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)