Olfactory Testing in Perinatal Asphyxia: Enhancing Risk Assessment

Recruiting Observational Study
Mild Birth Asphyxia Moderate Birth Asphyxia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
6 Hours – 72 Hours
Sex
Any
Study type
Observational
Participants needed
30 (estimated)
Sponsor
University of Parma · Other
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About This Trial
Neonatal asphyxia remains a leading cause of neurodevelopmental disabilities despite advancements in perinatal care. Hypoxic-ischemic encephalopathy (HIE), a severe outcome of asphyxia, impacts 1-3 infants per 1,000 live births annually in industrialized nations, causing long-term neurological impairments such as cognitive dysfunction, motor deficits, and sensory impairments. Early identification …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Term newborns (37-41 weeks of gestational age) with signs of asphyxia at birth (cord pH \< 7.10 and/or BE \> -12). * Maternal age \> 18 years. * No medication use during pregnancy (e.g., antipsychotics, antidepressants, sedatives, anticonvulsants, anxiolytics). * Absence of ma…
Contacts

Serafina Perrone, MD, PhD

3388704211

serafina.perrone@unipr.it

CONTACT