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Clinical Trials/NL-OMON50071
NL-OMON50071
Completed
Not Applicable

Cellular & Serological Immune Response Monitoring in SARS-CoV2-infected individuals, without need of hospitalization - SARS-RESPONSE

eids Universitair Medisch Centrum0 sites10 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Corona virus
Sponsor
eids Universitair Medisch Centrum
Enrollment
10
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • Subject (male or female) tested positive for SARS\-CoV2 by PCR (nasal swab,
  • throat swab and/or sputum);
  • Subject is an adult of 18\-65 years old;
  • Subject is able to understand the PIF document, written in Dutch;
  • Subject is able to communicate well with the investigator in the Dutch
  • Subject signed informed consent prior to any study\-mandated procedure;
  • Subject is living in Leiden or direct environment (e.g. within 10 km from
  • LUMC), allowing for traveling by car, bike or by walking to LUMC (no public
  • transportation).

Exclusion Criteria

  • Subject tested negative upon SARS\-CoV2 PCR re\-analysis of nasal swab at
  • Subject previously fainted before, during or after a medical procedure with
  • Subject received plasma or other blood products during the previous 3 months;
  • Subject received a vaccination during the previous 3 months;
  • Subject is obese with BMI \>\=30, based on provide weight and length information;
  • Subject has a pre\-existing coagulopathy;
  • Subject uses medication for a coagulopathy;
  • Subject uses medication that suppresses the immune system;
  • Subject has an auto\-immune disease or another immune disease;
  • Subject has another infection in addition to the SARS\-CoV2 infection;

Outcomes

Primary Outcomes

Not specified

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