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Recruiting NCT04615065

NCT04615065 Acutelines: a Large Data-/Biobank of Acute and Emergency Medicine

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Clinical Trial Summary
NCT ID NCT04615065
Status Recruiting
Phase
Sponsor University Medical Center Groningen
Condition Acute Disease
Study Type OBSERVATIONAL
Enrollment 35,000 participants
Start Date 2020-09-01
Primary Completion 2030-09-01

Trial Parameters

Condition Acute Disease
Sponsor University Medical Center Groningen
Study Type OBSERVATIONAL
Phase N/A
Enrollment 35,000
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2020-09-01
Completion 2030-09-01

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Brief Summary

Research in acute care faces many challenges, including enrollment challenges, legal limitations in data sharing, limited funding, and lack of singular ownership of the domain of acute care. To overcome some of these challenges, the Center of Acute Care of the University Medical Center Groningen in the Netherlands, has established a de novo data-, image- and biobank named "Acutelines". Acutelines is initiated to improve recognition and treatment of acute diseases and obtain insight in the consequences of acute diseases, including factors predicting its outcome. Thereby, Acutelines contributes to development of personalized treatment and improves prediction of patient outcomes after an acute admission.

Eligibility Criteria

Inclusion Criteria, at least one of the following: * Triaged as one of highest two triage categories (red or orange) according to the Manchester triage system; * Triaged as the third highest triage category (yellow) and arrival by EMS of Helicopter Emergency Medical Service (HEMS; * Shock * Suspicion of sepsis (based on either physicians' suspicion, Sepsis-2 or Sepsis-3 criteria) * Acute kidney injury (AKI) * Anaphylactic reaction * Syncope * Intoxication * Thrombosis * Pulmonary embolism * Bleeding while using anti-coagulant drugs * Gastro-intestinal bleeding * Electrolyte disturbance Exclusion Criteria: * Referred for organ transplantation as recipient * Transfer from other hospital * Accidental contact patient material (i.e. internal work-related accident) While data- and imaging will be collected from all these patients, biomaterials will only be collected from patients fulfilling the first criterion (i.e. triaged as one of highest two triage categories \[red or orange\] according

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