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CLEAR Sepsis Clinical Study

Noninvasive Hemodynamic Monitoring Utilizing ClearSight TM System in Suspected Sepsis Patients Presenting to the Emergency Department (CLEAR SEPSIS)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03231956
Acronym
CLEAR Sepsis
Enrollment
182
Registered
2017-07-27
Start date
2017-06-29
Completion date
2022-06-30
Last updated
2020-03-18

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

Conditions

Sepsis

Brief summary

To investigate the relationship between initial ClearSight™ derived hemodynamic parameters and outcomes (death, ongoing organ dysfunction or delayed ICU admission) in patients with acute infection and possible sepsis, with a focus on venous blood lactate (\< 2.0, 2.0-3.9, and ≥ 4.0 mmol/dL) and hemodynamic subgroups, using ED patients presenting with minor infections or asthma/COPD exacerbations as controls (henceforth referred to as Sepsis Mimic Group).

Interventions

DEVICEClearSight™ / EV1000NI Clinical Platform

Noninvasive Hemodynamic Monitoring utilizing ClearSight TM System

Sponsors

Edwards Lifesciences
Lead SponsorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Venous Blood Lactate Groups Inclusion Criteria: * ≥ 18 years of age at the time of enrollment * Any combination of acute symptoms and signs that the treating ED physician, after initial history and physical examination, attributes to a systemic infection * ED Physician confirms likely hospital admission (\> 50%) due to suspicion of infection * ED Physician confirms intention to order both blood cultures and venous blood lactate levels * Ability to enroll patient and begin ClearSight™ monitoring within three (3) hours of ED presentation

Exclusion criteria

* Initial venous blood lactate measured \> 3 hours after ED arrival * Pre-existing infection for which patient is being treated with antibiotics as an outpatient * Prisoners * Pregnant women * Any previous medical condition with life expectancy of \< 3 months (patients with ESRD and heart failure are not excluded) * DNR or comfort care order preexisting to ED visit or established in the ED * Palliative care or hospice consult in the ED * Known severe aortic insufficiency * Known history of Raynaud's disease * Poor follow-up candidate in the opinion of the Investigator * Current or planned enrollment in an investigational trial that in the opinion of the Investigator may significantly affect hemodynamic data collection. Control Sepsis Mimic Inclusion Criteria: * ≥18 years of age at the time of enrollment * Presents to the ED with a chief complaint consistent with a minor infection (upper respiratory infection, soft tissue infection, viral infection) or an asthma or COPD exacerbation on whom the treating physician is not ordering labs for blood cultures or lactate levels * Ability to enroll patient and begin ClearSight™ monitoring within three (3) hours of ED presentation.

Design outcomes

Primary

MeasureTime frameDescription
Composite outcomeWithin 72 hours of presentationIncrease in modified Sequential Organ Failure Assessment (mSOFA) score ≥ 1 resulting in ICU admission / death.
Venous Blood Lactate clearanceWithin 24 and 72 hours of presentationVenous Blood Lactate clearance
Length of Stay30 daysEmergency Department length of stay, ICU length of stay, and Hospital length of stay
Recidivism30 daysRecidivism within 30 days of the index hospital visit

Countries

United States

Contacts

Primary ContactJurandir Araujo, BA
jurandir_araujo@edwards.com949-250-5469
Backup ContactRyan Zafra, BS
ryan_zafra@edwards.com949-250-1354

Outcome results

None listed

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