Actively Recruiting

Age: 0Years +
All Genders
ID04459689

Worldwide COVID-19 in Children and Adult Patients With Primary ImmunoDeficiencies (PID) Survey

Led by Imagine Institute · Updated on 2025-03-05

200

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the impact of COVID-19 infection on individuals with primary immunodeficiencies (PID), a group for which little information currently exists. The study builds on an earlier survey phase and aims to gather detailed data on how COVID-19 affects survival, hospitalizations, and oxygen therapy needs among PID patients. This observational survey is conducted through a secure online platform and involves global participation by healthcare professionals. The study collects retrospective data from health care providers who enter patient information on a GDPR-compliant system. It focuses on patients of all ages diagnosed with PID and affected by COVID-19. The survey gathers extensive clinical details to better understand outcomes such as ICU admissions and post-infection sequelae. Participants are represented by their healthcare providers who document various outcomes including survival, ICU admission rates, and oxygen therapy use at baseline, as well as longer-term effects. The study began in March 2020 and will continue through February 2027. The data collection is designed to adapt as new knowledge of the pandemic emerges, enhancing understanding of COVID-19's effects on this vulnerable population.

CONDITIONS

Brief Title

COVID-19 in PID Survey

Who Can Participate

Age: 0Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with a Primary Immune Deficiency
  • Proven or probable COVID-19 infection
Not Eligible

You will not qualify if you...

  • Secondary Immune Deficiency
  • Other Coronavirus infection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surveillance

Duration - Up to 5 years

Participants who have Primary Immune Deficiency and COVID-19 infection are observed to collect data on their health outcomes.

Trial Site Locations

Total: 1 location

1

Imagine Institute

Paris, France, 75015

Actively Recruiting

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Research Team

N

Nizar MAHLAOUI, MD, MPH, PhD

H

Hassan FAOUR, BS

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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