Echo vs. EGDT in Severe Sepsis and Septic Shock

NCT ID: NCT02354742

Last Updated: 2018-07-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-12-31

Study Completion Date

2017-10-31

Brief Summary

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Echocardiography (cardiac ultrasound) is being used more often in the critical care setting for management of severe infection (septic shock). Early studies show echocardiography to be useful in these patients, but at this time, there are no good clinical trials to justify its use.

Our study goals/objectives are as follows:

1. To conduct an unblinded, two-group randomized controlled clinical trial to compare an echocardiography-guided resuscitation protocol with an Early Goal Directed Therapy (EGDT) protocol in patients with severe sepsis or septic shock.
2. Demonstrate that a sepsis treatment protocol using transthoracic echocardiography and other non-invasive assessments of cardiac output will result in more rapid resolution of septic shock compared to invasive EGDT.
3. Demonstrate patients receiving the non-invasive echocardiography protocol will receive less administration of intravenous fluid.

Detailed Description

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Conditions

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Severe Sepsis Septic Shock

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Early Goal Directed Therapy (EGDT)

EGDT is currently standard of care in management of septic shock, so assignment to this treatment arm will confer no additional risk above that of standard of care. EGDT utilizes placement of a central venous catheter, an arterial catheter, and administration of intravenous fluid and vasoactive medications. EGDT uses central venous catheter to assess central venous pressure and ScVO2.

Group Type ACTIVE_COMPARATOR

EGDT fluid resuscitation

Intervention Type OTHER

Patients will have their fluid resuscitation care guided by an EGDT protocol, which is currently used as standard of care.

Echo Guided Fluid Resuscitation

The echo arm also utilizes placement of a central venous catheter, an arterial catheter, and administration of intravenous fluid and vasoactive medications, all of which are interventions found in standard care. The central venous pressure will not be monitored in this arm. Instead, decisions for giving fluids will be directed by the results of Echocardiography. Echocardiography poses no known risk to the patient, and it is non-invasive. The only risk of echocardiography is that of misdiagnosis.

Group Type EXPERIMENTAL

Echo guided fluid resuscitation

Intervention Type OTHER

Patients will have their fluid resuscitation care guided by measurements obtained during an echo.

Interventions

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Echo guided fluid resuscitation

Patients will have their fluid resuscitation care guided by measurements obtained during an echo.

Intervention Type OTHER

EGDT fluid resuscitation

Patients will have their fluid resuscitation care guided by an EGDT protocol, which is currently used as standard of care.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* At least 18 years of age
* Suspected infection
* Two or more systemic inflammatory response syndrome (SIRS) criteria

* White blood cell count less than 4,000 per mm3, greater than 12,000 per mm3, or differential with greater than 10% immature forms
* Heart rate greater than 90 beats per minute
* Respiratory rate greater than 20 breaths per minute or paCO2 less than 32 mmHg
* Temperature less than 36°C or greater than 38°C
* Evidence of refractory hypoperfusion attributed to sepsis (one or more of the following):

* Systolic blood pressure less than 90 mmHg despite an intravenous fluid challenge of at least 30ml/kg (a portion of this may be albumin equivalent)
* Blood lactate level at least 4 mmol/L.
* Intention to place an arterial catheter.
* Intention to place a central venous catheter.

Exclusion Criteria

* Known pregnancy
* Requirement for immediate surgery
* Hypotension attributed to alternative cause
* Treating physician deems the patient is moribund
* Treating physician deems aggressive care is unsuitable
* Contraindication to central venous catheterization or arterial catheterization
* Advanced directives restricting implementation of the protocol
* Significant pathology of the chest or abdominal wall that would make transthoracic echocardiography impossible (burns, chest trauma, etc.)
* Children under the age of 18 will not be included in this study
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Intermountain Health Care, Inc.

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Michael Lanspa, MD

Role: PRINCIPAL_INVESTIGATOR

Intermountain Health Care, Inc.

Locations

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Intermountain Medical Center

Murray, Utah, United States

Site Status

Countries

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United States

References

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Lanspa MJ, Burk RE, Wilson EL, Hirshberg EL, Grissom CK, Brown SM. Echocardiogram-guided resuscitation versus early goal-directed therapy in the treatment of septic shock: a randomized, controlled, feasibility trial. J Intensive Care. 2018 Aug 13;6:50. doi: 10.1186/s40560-018-0319-3. eCollection 2018.

Reference Type DERIVED
PMID: 30123511 (View on PubMed)

Other Identifiers

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1024925

Identifier Type: -

Identifier Source: org_study_id

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