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Study identifier: NCT06434701 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Severe COVID-19 Infection in Children Presenting to EDs in Israel and England

Condition: COVID-19 · Inflammatory Response  ·  Sponsor: Hadassah Medical Organization

PhaseNA
Planned participants500
Who can joinAll sexes, 0 Years to 16 Years
Healthy volunteersNo

About this study

Even though the COVID-19 pandemic is no longer at its peak, the threat still lingers. Engaging in prospective surveillance studies will enable us to monitor the disease and prepare for any potential resurgence. COVID-19 surveillance studies are essential tools for policymakers to make informed decisions, allocate resources, and develop strategies to control the spread of the virus and protect public health. The objective of this surveillance study is to prospectively assess in-hospital severe morbidity related to COVID-19 infection in children who present to the Pediatric Emergency Department (ED). A prospective multicenter study will be conducted across eight EDs in Israel and five EDs in the United Kingdom. The study population will include children aged 16 years or younger with a severe acute COVID-19 infection. Confirmation of acute COVID-19 infection will be based on polymerase chain reaction nasopharyngeal swab testing. The study will also include patients diagnosed with multisystem inflammatory syndrome in children (MIS-C), as defined by the CDC.

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

Talk to the study team

Itai Shavit, MD  ·  00 972 50 2063239  ·  shavit1@hadassah.org.il

Hadas Lamberg, PhD  ·  00 972 2 6777572  ·  lhadas@hadassah.org.il

Always discuss trial participation with your own doctor first.

Locations (6)

Haemek Medical CenterAfula, IsraelRecruiting
Soroka Medical CenterBeersheba, IsraelRecruiting
Hadassah Medical CenterJerusalem, IsraelRecruiting
Shaare Zedek Medical CenterJerusalem, IsraelRecruiting
Meir Medical CenterKfar Saba, IsraelRecruiting
Sheba Medical CenterTel Litwinsky, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06434701