Skip to content

Registry of COVID-19 Patients at AOUI Verona

Registry of Biological Samples, Clinical Information and Epidemiological Data of COVID-19 Patients Admitted at the University Hospital of Verona (AOUI Verona)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04497194
Enrollment
430
Registered
2020-08-04
Start date
2020-03-01
Completion date
2020-09-30
Last updated
2021-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronavirus Disease 2019

Brief summary

The registry of COVID-19 patients was designed to collect epidemiolgical, demographic, clinical, anamnestic and outcome information together with serological and microbiological samples from COVID-19 patients admitted at the University Hospital of Verona (Azienda Ospedaliera Universitaria Integrata, AOUI Verona). All SARS-CoV 2 positive patients admitted and able to give an informed consent are included, irrespectively of age and gender.

Detailed description

Anamnestic data are collected at the enrollment, while all the other clinical and epidemiological information are retrieved retrospectively from patients' medical records and electronic health records. Serological and microbiological samples (blood samples, fecal samples and nasal/rectal swabs) are collected within 48 hours after admission and during the hospital stay, according with routine internal procedures.The biological samples are stored at the University Laboratory for Medical Research (Laboratorio Universitario di Ricerca Medica, LURM). A dedicated database has been created and implemented to collect all the above mentioned information.

Interventions

not applicable (observational study)

Sponsors

Azienda Ospedaliera Universitaria Integrata Verona
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL

Inclusion criteria

* PCR for SARS-CoV 2 positive on NPS swab or high suspicion of SARS-CoV 2 with ongoing swab; * All ages; * All genders; * Informed consent obtained.

Exclusion criteria

* Failure to obtain the informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Epidemiological predictors of poor outcomes in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsEpidemiological data including demographic data, contact with COVD-19 positive patients and onset of symptoms.
Clinical predictors of poor outcomes in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsUnderlying chronic diseases, signs/symptoms related with COVID-19 diseases an clinical presentation on admission
Body temperature (°C) on admission in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsBody temperature (°C)
Blood pressure (mmHg) on admission in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsBlood pressure (mmHg)
Pulse rate (beats per minute) on admission in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsPulse rate (beats per minute)
Respiratory rate (breaths per minute) on admission in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsPulse rate (beats per minute)
Peripheral oxygen saturation (%) on admission in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsPeripheral oxygen saturation (%)
C reactive protein (CRP, m/gL) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsCRP (m/gL)
Procalcitonin (PCT, ng/mL) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsPCT (ng/mL
White Blood Count (WBC, cell/mm3) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsWhite Blood Count (WBC, cell/mm3)
Neutrophils (cell/mm3) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsNeutrophils (cell/mm3)
Lymphocytes (cell/mm3) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsLymphocytes (cell/mm3)
Platelets (cell/mm3) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsPlatelets (cell/mm3)
L-lattato deidrogenasi (LDH, mU/ml) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsLDH (mU/ml)
Creatine kinase (CK, U/L) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsCK (U/L)
D-dimer (μg/L) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsD-dimer (μg/L)
fibrinogen (g/L) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsfibrinogen (g/L)
ferritin (mcg/L) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsferritin (mcg/L)
AST (U/L) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsAST (U/L)
ALT (U/L) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsALT (U/L)
Creatinine (mg/dl) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsCreatinine (mg/dl)
Arterial blood gas anaysis pH in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthspH
Arterial blood gas anaysis pO2 (mmHg) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthspO2 (mmHg)
Arterial blood gas anaysis pCO2 (mmHg) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthspCO2 (mmHg)
Arterial blood gas anaysis HCO3 (mmol/l) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsHCO3 (mmol/l)
Arterial blood gas anaysis SpO2 (%) in COVID-19 patients admitted to University Hospital of Veronathrough study completion, an average of 3 monthsSpO2 (%)
Host-related factors associated with the pathogenesis of COVID-19through study completion, an average of 3 monthsIL-6 (pg/mL)
Virological factors associated with the pathogenesis of COVID-19through study completion, an average of 3 monthsNasal and rectal swabs, fecal samples and blood samples

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026