Skip to content

Evaluation with ultrasound on the bedside in serious patients with COVID-19

Evaluation with point-of-care ultrasound in serious patients with COVID-19 - POCUS COVID-19: point-of-care ultrasound for covid-19

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
REBEC
Registry ID
RBR-43hbks
Enrollment
Unknown
Registered
2020-06-03
Start date
2020-04-21
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Severe Acute Respiratory Syndrome

Interventions

The only intervention proposed by the study is an evaluation with point-of-care ultrasonography (at the bedside) mainly for analysis of possible central access sites in pronated patients. There is no
Drug
Procedure/surgery
Other

Sponsors

Disciplina de Cirurgia Vascular e Endovascular da Universidade Federal de São Paulo
Lead Sponsor
Disciplina de Cirurgia Vascular e Endovascular da Universidade Federal de São Paulo
Collaborator

Eligibility

Age
No minimum to 130 Years

Inclusion criteria

Inclusion criteria: patients admitted to the intensive care unit with a confirmed Covid-19 diagnosis

Exclusion criteria

Exclusion criteria: covid-19 suspect patient (not yet confirmed)

Design outcomes

Primary

MeasureTime frame
It is expected to find new sites for the passage of central venous access for critically ill patients with COVID 19. It is intended to present the number and possible parameters for central venous access in pronated patients.

Secondary

MeasureTime frame
It is intended to assess the prevalence of deep venous thrombosis (%), using B-mode ultrasound at the bedside (point-of-care).

Countries

Brazil

Contacts

Public ContactLuis;Ronald Nakano;Flumignan

Disciplina de Cirurgia Vascular e Endovascular da Universidade Federal de São Paulo;Disciplina de Cirurgia Vascular e Endovascular da Universidade Federal de São Paulo

luiscnakano@uol.com.br;flumignan@gmail.com+551155764848;1155764848

Outcome results

None listed

Source: REBEC (via WHO ICTRP)