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Evaluation of Serial Ultrasound Screening in ICU COVID-19 Patients

Primary Purpose

Deep Vein Thrombosis, Covid19, COVID-19 Pneumonia

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
venous ultrasound of lower extremity
Sponsored by
Hospital Universitari Vall d'Hebron Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Deep Vein Thrombosis focused on measuring covid19, pulmonary embolism, intensive care unit, deep venous thrombosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • COVID 19 patients in their dirst 72 hours of entering ICU

Exclusion Criteria:

  • Pregnant patients
  • Not COVID 19 confirmed patients by PCR
  • Patients that are in Extracorporeal membrane oxygenation
  • Patients with previous thrombotic disease

Sites / Locations

  • Hospital Universitari Vall d'HebronRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention group

control group

Arm Description

Selected patients undego lower extremity ultrasound for diagnosis of deep vein thrombosis 2 times per week (mondays and thursdays) in a period of 3 weeks (21 days) of follow up

This group only undergo the first ultrasound assesment to discard previos thrombosis not detected during hospitalization or ambulatory

Outcomes

Primary Outcome Measures

Mortality
Patients that die in ICU during follow up
ICU Stay
Number of days staying in that unit during follow up

Secondary Outcome Measures

Full Information

First Posted
August 30, 2021
Last Updated
August 30, 2021
Sponsor
Hospital Universitari Vall d'Hebron Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05028244
Brief Title
Evaluation of Serial Ultrasound Screening in ICU COVID-19 Patients
Official Title
Evaluation of Serial Ultrasound Screening for Lower Extremity Deep Vein Thrombosis in Patients With COVID-19 Admitted to Intensive Care.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 15, 2021 (Actual)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
March 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Universitari Vall d'Hebron Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This clinical trial is destinated to evaluate if the periodic screening for deep venous thrombosis by ultrasound of lower extremity in patients with intensive care unit (ICU) patients with COVID 19 impacts on mortality, ICU stay and total lenght of stay in the hospital, along with other outcomes.
Detailed Description
Background: COVID-19 has a high incidence of venous thromboembolic disease (VTE), especially pulmonary thromboembolism (PE) and deep vein thrombosis (DVT), with an even higher incidence in patients admitted to the intensive care unit (ICU). The presentation of these events is related to an increase in mortality and the mean stay in the ICU. The impact of systematic screening for asymptomatic lower extremity DVT in these patients has not been studied, so we propose to carry out a clinical trial to assess its impact in these patients. Hypothesis: Serial DVT screening in patients admitted to the ICU for COVID-19 does not improve survival, mean stay, or the incidence of symptomatic VTE. Objective: To study whether DVT screening in these patients has an impact on the incidence of symptomatic VTE, mortality and average stay in the ICU. Methods: Non-blind randomized clinical trial on all patients aged 18 years or older admitted to the ICU for COVID-19 with less than 72 hours elapsed since their admission to the unit. Patients with DVT or PE will be excluded at the time of recruitment (all patients will be ruled out by routine ultrasound and computed tomography angiography (CT Angiography)); Pregnant patients, patients with a previous diagnosis of DVT or PE, and patients undergoing extracorporeal membrane oxygenation (ECMO) will also be excluded. Patients will be randomized into two arms at the time of inclusion: the screened group (Group 1) and the non-screened group (Group 2). Group 1: patients who will be treated according to the usual ICU protocol and, additionally, will undergo serial ultrasounds of the lower extremities twice a week (Monday and Thursday). Group 2: they will be treated according to the usual ICU protocol and no screening examinations will be performed. Patients will be followed until discharge from the ICU or death and up to a maximum of 3 weeks. The incidence of symptomatic VTE will be assessed, as well as all-cause mortality and days of stay in the ICU. Clinical and laboratory variables will be collected from each patient for subsequent statistical analysis. Relevance: The thrombotic complications of COVID-19 are well described, as well as their high incidence in critically ill patients. This work aims to clarify the current doubts about the need for systematic DVT screening in these patients. If our hypothesis is verified, a limited resource such as ultrasound of the lower limbs could be saved, as well as the use of the necessary protection materials and, most importantly, avoid unnecessary exposure of health personnel with the consequent risk that it represents for other professionals and patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep Vein Thrombosis, Covid19, COVID-19 Pneumonia, COVID-19 Respiratory Infection, COVID-19 Acute Respiratory Distress Syndrome, COVID-19 Acute Bronchitis, COVID-19 Lower Respiratory Infection, Pulmonary Embolism
Keywords
covid19, pulmonary embolism, intensive care unit, deep venous thrombosis

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The selected patients undergo an ultrasound of lower extremity to discard previous thrombosis episodes. Then they are randomized to an intervention group (serial screening of deep venous thrombosis in lower extremity 2 times per week) or control group (no other exploration or interventions are made).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
170 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Selected patients undego lower extremity ultrasound for diagnosis of deep vein thrombosis 2 times per week (mondays and thursdays) in a period of 3 weeks (21 days) of follow up
Arm Title
control group
Arm Type
No Intervention
Arm Description
This group only undergo the first ultrasound assesment to discard previos thrombosis not detected during hospitalization or ambulatory
Intervention Type
Diagnostic Test
Intervention Name(s)
venous ultrasound of lower extremity
Intervention Description
Patients inbed are explored for deep vein thrombosis in femoral-popliteal and distal veins of the legs with ultrasound compresión and doppler flow evaluation
Primary Outcome Measure Information:
Title
Mortality
Description
Patients that die in ICU during follow up
Time Frame
21 days
Title
ICU Stay
Description
Number of days staying in that unit during follow up
Time Frame
21 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: COVID 19 patients in their dirst 72 hours of entering ICU Exclusion Criteria: Pregnant patients Not COVID 19 confirmed patients by PCR Patients that are in Extracorporeal membrane oxygenation Patients with previous thrombotic disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sergi Bellmunt Montoya
Phone
34934894010
Email
sbellmunt@vhebron.net
First Name & Middle Initial & Last Name or Official Title & Degree
Carlos Marrero Eligio de la Puente
Phone
34637348532
Email
cmarrero@vhebron.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sergi Bellmunt Montoya
Organizational Affiliation
Hospital Vall d'Hebron
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitari Vall d'Hebron
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sergi Bellmunt Montoya
Phone
34637348532
Email
sbellmunt@vhebron.net
First Name & Middle Initial & Last Name & Degree
Carlos Marrero Eligio de la Puente
Phone
34637348532
Email
cmarrero@vhebron.net

12. IPD Sharing Statement

Plan to Share IPD
No

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Evaluation of Serial Ultrasound Screening in ICU COVID-19 Patients

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