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UnknownNCT03208257

Esmolol to Control Adrenergic Storm in Septic Shock- ROLL-IN 2

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
10 (estimated)
Sponsor
Samuel Brown · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Septic shock is a common syndrome caused by the body's response to an infection. Septic shock is responsible for 10% of all ICU admissions and 30% of ICU deaths. Use of "beta blocker" medications may improve outcomes after septic shock. This pilot study evaluates protocols to infuse the beta blocker esmolol in patients with septic shock.

Detailed description

This is a prospective, single arm, feasibility study of esmolol infusion in septic shock. The objective is to evaluate the feasibility, adequacy, and efficiency of study protocols for a subsequent ECASSS study. This study (ECASSS-R2) extends observations made in an initial pilot, ECASSS-R.

Conditions

Interventions

TypeNameDescription
DRUGEsmololEsmolol hydrochloride infusion

Timeline

Start date
2017-08-07
Primary completion
2020-12-01
Completion
2021-06-01
First posted
2017-07-05
Last updated
2019-02-26

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03208257. Inclusion in this directory is not an endorsement.

Esmolol to Control Adrenergic Storm in Septic Shock- ROLL-IN 2 (NCT03208257) · Clinical Trials Directory