Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
574 participants
OBSERVATIONAL
2020-08-01
2022-03-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Rapid Diagnostic Profiling of SARS-CoV-2 (COVID-19)
NCT04473365
COVID-19 Quick Start - Test and Treat in Africa
NCT06360783
Observational Study of the Clinico-biological Evolution and Standard of Care Offered to Patients With Ebola Virus Disease
NCT04815174
Clinical Outcomes of paTients pREsenting to HArare COVID-19 CenTer of Excellence With SARS-CoV-2 Infection
NCT05529771
Collection of Tissue Specimens in Mali, West Africa, for HIV and Tuberculosis Research
NCT00341042
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Patients hospitalized and positive for COVID-19 by PCR and their household contacts of all ages and gender (40% minimum of female), will be enrolled upon receipt of written informed consent.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Index cases
Patients infected by SARS-Cov2 Polymerase Chain Reaction (PCR) and hospitalized in a referral center for COVID-19 .
No interventions assigned to this group
Households cases
Household contacts of SARS-Cov2 hospitalized COVID-19 patients.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Household contacts of hospitalized COVID-19 patient,
* Provided signed informed consent.
Exclusion Criteria
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
European and Developing Countries Clinical Trials Partnership (EDCTP)
OTHER_GOV
Leiden University Medical Center
OTHER
Institut de recherche en santé de surveillance épidémiologique et de formation
UNKNOWN
Université des Sciences de la Santé
UNKNOWN
Armauer Hansen Research Institute, Ethiopia
OTHER
Universität Tübingen
OTHER
Centre de Recherche Médicale de Lambaréné
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Ayôla Akim ADEGNIKA
Role: PRINCIPAL_INVESTIGATOR
Centre de Recherches Médicales de Lambaréné
Marielle BOUYOU-AKOTET
Role: PRINCIPAL_INVESTIGATOR
Université des Sciences de Santé
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Centre de Recherches Médicales de Lammbaréné
Lambaréné, Moyen-Ogooué Province, Gabon
Centre de Recherches Médicales de Lambréné
Lambaréne, , Gabon
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CEI-10/2020
Identifier Type: OTHER
Identifier Source: secondary_id
0011/2020/PR/SG/CNE
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.