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Study identifier: NCT04459689 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

COVID-19 in PID Survey

Condition: Primary Immune Deficiency · COVID  ·  Sponsor: Imagine Institute

PhaseN/A
Planned participants200
Who can joinAll sexes, 0 Years to no upper limit
Healthy volunteersNo

About this study

With the emergence of SARS-CoV-2 and the COVID-19 pandemic, there is an urgent need to understand the impact of infection on immunodeficient individuals. Whilst co-morbidities (such as diabetes, cancer, arterial hypertension, heart disease...) have been documented in people infected with SARS-CoV-2, there is currently no information on the consequences and outcomes for individuals with primary immunodeficiencies (PID). Following the 1st phase of the survey (launched by Isabelle Meyts (ESID), Nizar Mahlaoui (CEREDIH \& IPOPI) and Kate Sullivan with Stuart Tangye (IUIS), that gave an idea of the number of affected PID patients and the impact of SARS-CoV-2 and directly focusing on obtaining this top level of information), we are launching the 2nd phase: "COPID19". COPID19 survey is a secured online GDPR compliant platform based in Paris (Imagine Institute). It has been approved by the Paris-Necker-Enfants malades IRB and Ethics Committee. However, this retrospective survey is designed for global distribution. Data can be entered by a health care professional (mostly clinicians) through a personal login and password. Each documenting person will have access to his/her own patients' data. COPID19 require a greater level of information than the 1st phase. The eCRF will be open to evolutions depending on progresses in our knowledge of this pandemic.

This description comes directly from the study's public registry record.

Talk to the study team

Nizar MAHLAOUI, MD, MPH, PhD  ·  +33144494622  ·  nizar.mahlaoui@aphp.fr

Hassan FAOUR, BS  ·  +33 1 42 75 44 73  ·  supportdatabase@institutimagine.org

Always discuss trial participation with your own doctor first.

Locations (1)

Imagine InstituteParis, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT04459689