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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04741412
Other study ID # 212_20 B
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 3, 2020
Est. completion date May 31, 2021

Study information

Verified date August 2021
Source University Hospital Erlangen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Longitudinal study of 56 households with at least one member who had COVID-19 to compare the course of illness, immune responses, and long-term consequences of SARS-CoV-2 infection in HED patients with those of control subjects of the same age group. Complete households are investigated, including women who are pregnant when exposed to the virus and their newborn child(ren).


Recruitment information / eligibility

Status Completed
Enrollment 231
Est. completion date May 31, 2021
Est. primary completion date May 31, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - household with one or more members registered as patient(s) in the University Hospital Erlangen - at least one person <18 years of age - at least one household member who has or had a SARS-CoV-2 infection confirmed by a positive PCR test, detection of specific antibodies against this virus, or by development of COVID-19 symptoms after being in close contact with a person known to be infected with SARS-CoV-2 - informed consent Exclusion Criteria: - missing informed consent of one or more household members - language barriers to communication that would prevent informed consent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany University Hospital Erlangen Erlangen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Erlangen

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary age-dependence of SARS-CoV-2 infection registry of household members with and without symptoms of COVID-19 (entire households) 3 months from the point in time at which the first household member shows symptoms of COVID-19
Primary percentage of household members infected by SARS-CoV-2 The infection rate is determined on the basis of specific PCR tests and detectibility of antibodies against SARS-CoV-2. 3 months from the point in time at which the first household member shows symptoms of COVID-19
Primary duration of primary COVID-19 symptoms The possible association between the length of time with symptoms of COVID-19 and specific immune responses, in particular the development of virus-neutralizing antibodies, is studied. 2 months from the onset of COVID-19 symptoms
Primary frequency of late-onset cardiovascular complications Patient-reported known and yet unknown long-term consequences of COVID-19 are registered and investigated further (questionnaire, specific data confirmed by clinical examination). 2-12 months from the onset of COVID-19 symptoms
Primary frequency of postviral fatigue Patient-reported symptoms of fatigue are registered (questionnaire). 2-12 months from the onset of COVID-19 symptoms
Primary frequency of noticeable temporary hair loss after COVID-19 Patient-reported extent of hair loss is registered (questionnaire). 2-12 months from the onset of COVID-19 symptoms
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